Harnessing Cell Membrane-Derived Nanovesicles for Enhanced Nanoprobes in Multimodal Imaging: Progress and Perspectives

Lingling Lei , Meng Du , Jianjian Zhang , Yuguang Mu

BIO Integration ›› 2025, Vol. 6 ›› Issue (1) : 28

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BIO Integration ›› 2025, Vol. 6 ›› Issue (1) :28 DOI: 10.15212/bioi-2025-0047
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Harnessing Cell Membrane-Derived Nanovesicles for Enhanced Nanoprobes in Multimodal Imaging: Progress and Perspectives
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Abstract

Cell membrane-derived nanovesicles (CMNVs) are natural nanocarriers efficiently encapsulating bioactive molecules and imaging probes. Conventional nanoprobes face challenges, like rapid immune clearance, off-target accumulation, and long-term toxicity. CMNVs overcome these challenges by leveraging inherent biofunctionalization. CMNVs enhance encapsulated nanoprobe targeting, prolong circulation, boost specific tissue accumulation, and improve imaging precision through inherited membrane proteins or minimally disruptive exogenous modifications. CMNVs show significant promise across multiple imaging modalities, including fluorescence, bioluminescence, photoacoustic, and MRI. This review systematically evaluates the limitations of traditional nanoprobes, highlights the unique advantages of CMNVs in enhancing diverse probe performance, discusses current challenges in harnessing CMNVs for imaging, and provides insights for developing future high-precision imaging strategies.

Keywords

Bioluminescence / cell membrane-derived nanovesicles / MRI / nanoprobes / fluorescence / photoacoustic imaging

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Lingling Lei, Meng Du, Jianjian Zhang, Yuguang Mu. Harnessing Cell Membrane-Derived Nanovesicles for Enhanced Nanoprobes in Multimodal Imaging: Progress and Perspectives. BIO Integration, 2025, 6 (1) : 28 DOI:10.15212/bioi-2025-0047

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References

[1]

Deng H, Li LX, Ju J, Mo X, Ge G, et al. Multifunctional nanoprobes for macrophage imaging. Biomaterials 2022; 290: 121824. [PMID: 36209580 DOI: 10.1016/j.biomaterials.2022.121824]

[2]

Li S, Wei J, Yao Q, Song X, Xie J, et al. Emerging ultrasmall luminescent nanoprobes for in vivo bioimaging. Chem Soc Rev 2023; 52(5): 1672-96. [PMID: 36779305 DOI: 10.1039/d2cs00497f]

[3]

Xiao W, Gao H. The impact of protein corona on the behavior and targeting capability of nanoparticle-based delivery system. Int J Pharm 2018; 552(1-2): 328-39. [PMID: 30308270 DOI: 10.1016/j.ijpharm.2018.10.011]

[4]

Song Y, Feng D, Shi W, Li X, Ma H. Parallel comparative studies on the toxic effects of unmodified CdTe quantum dots, gold nanoparticles, and carbon nanodots on live cells as well as green gram sprouts. Talanta 2013; 116: 237-44. [PMID: 24148399 DOI: 10.1016/j.talanta.2013.05.022]

[5]

Llop J, Lammers T. Nanoparticles for cancer diagnosis, radionuclide therapy and theranostics. ACS Nano 2021; 15(11): 16974-81. [PMID: 34748314 DOI: 10.1021/acsnano.1c09139]

[6]

Zhou Y, Dai Z. New strategies in the design of nanomedicines to oppose uptake by the mononuclear phagocyte system and enhance cancer therapeutic efficacy. Chem Asian J 2018; 13(22): 3333-40. [PMID: 29441706 DOI: 10.1002/asia.201800149]

[7]

Hu T, Huang Y, Liu J, Shen C, Wu F, et al. Biomimetic cell-derived nanoparticles: emerging platforms for cancer immunotherapy. Pharmaceutics 2023; 15(7): 1821. [PMID: 37514008 DOI: 10.3390/pharmaceutics15071821]

[8]

Hong G, Robinson JT, Zhang Y, Diao S, Antaris AL, et al. In vivo fluorescence imaging with Ag2S quantum dots in the second near-infrared region. Angew Chem Int Ed Engl 2012; 51(39): 9818-21. [PMID: 22951900 DOI: 10.1002/anie.201206059]

[9]

Choi HS, Liu W, Misra P, Tanaka E, Zimmer JP, et al. Renal clearance of quantum dots. Nat Biotechnol 2007; 25(10): 1165-70. [PMID: 17891134 DOI: 10.1038/nbt1340]

[10]

Fitzpatrick JAJ, Andreko SK, Ernst LA, Waggoner AS, Ballou B, et al. Long-term persistence and spectral blue shifting of quantum dots in vivo. Nano Lett 2009; 9(7): 2736-41. [PMID: 19518087 DOI: 10.1021/nl901534q]

[11]

Antaris AL, Chen H, Cheng K, Sun Y, Hong G, et al. A small-molecule dye for NIR-II imaging. Nat Mater 2016; 15(2): 235-42. [PMID: 26595119 DOI: 10.1038/nmat4476]

[12]

Luo W, Dai Y, Chen Z, Yue X, Andrade-Powell KC, et al. Spatial and temporal tracking of cardiac exosomes in mouse using a nano-luciferase-CD63 fusion protein. Commun Biol 2020; 3(1): 114. [PMID: 32157172 DOI: 10.1038/s42003-020-0830-7]

[13]

Gujrati V, Prakash J, Malekzadeh-Najafabadi J, Stiel A, Klemm U, et al. Bioengineered bacterial vesicles as biological nano-heaters for optoacoustic imaging. Nat Commun 2019; 10(1): 1114. [PMID: 30846699 DOI: 10.1038/s41467-019-09034-y]

[14]

Zhu D, Li Y, Zhang Z, Xue Z, Hua Z, et al. Recent advances of nanotechnology-based tumor vessel-targeting strategies. J Nanobiotechnology 2021; 19(1): 435. [PMID: 34930293 DOI: 10.1186/s12951-021-01190-y]

[15]

Lv Y, Liu M, Zhang Y, Wang X, Zhang F, et al. Cancer cell membrane-biomimetic nanoprobes with two-photon excitation and near-infrared emission for intravital tumor fluorescence imaging. ACS Nano 2018; 12(2): 1350-8. [PMID: 29338190 DOI: 10.1021/acsnano.7b07716]

[16]

Legrand N, Huntington ND, Nagasawa M, Bakker AQ, Schotte R, et al. Functional CD47/signal regulatory protein alpha (SIRP(alpha)) interaction is required for optimal human T- and natural killer- (NK) cell homeostasis in vivo. Proc Natl Acad Sci U S A 2011; 108(32): 13224-9. [PMID: 21788504 DOI: 10.1073/pnas.1101398108]

[17]

Pan S, Zhang Y, Huang M, Deng Z, Zhang A, et al. Urinary exosomes-based engineered nanovectors for homologously targeted chemo-chemodynamic prostate cancer therapy via abrogating EGFR/AKT/NF-kB/IkB signaling. Biomaterials 2021; 275: 120946. [PMID: 34119884 DOI: 10.1016/j.biomaterials.2021.120946]

[18]

Reuveni T, Motiei M, Romman Z, Popovtzer A, Popovtzer R. Targeted gold nanoparticles enable molecular CT imaging of cancer: an in vivo study. Int J Nanomedicine 2011; 6: 2859-64. [PMID: 22131831 DOI: 10.2147/IJN.S25446]

[19]

Khademi S, Sarkar S, Shakeri-Zadeh A, Attaran N, Kharrazi S, et al. Targeted gold nanoparticles enable molecular CT imaging of head and neck cancer: An in vivo study. Int J Biochem Cell Biol 2019; 114: 105554. [PMID: 31276787 DOI: 10.1016/j.biocel.2019.06.002]

[20]

Ma L, Liu T-W, Wallig MA, Dobrucki IT, Dobrucki LW, et al. Efficient targeting of adipose tissue macrophages in obesity with polysaccharide nanocarriers. ACS Nano 2016; 10(7): 6952-62. [PMID: 27281538 DOI: 10.1021/acsnano.6b02878]

[21]

Suk JS, Xu Q, Kim N, Hanes J, Ensign LM. PEGylation as a strategy for improving nanoparticle-based drug and gene delivery. Adv Drug Deliv Rev 2016; 99(Pt A): 28-51. [PMID: 26456916 DOI: 10.1016/j.addr.2015.09.012]

[22]

Zhang P, Sun F, Liu S, Jiang S. Anti-PEG antibodies in the clinic: Current issues and beyond PEGylation. J Control Release 2016; 244(Pt B): 184-93. [PMID: 27369864 DOI: 10.1016/j.jconrel.2016.06.040]

[23]

Yang Q, Lai SK. Anti-PEG immunity: emergence, characteristics, and unaddressed questions. Wiley Interdiscip Rev Nanomed Nanobiotechnol 2015; 7(5): 655-77. [PMID: 25707913 DOI: 10.1002/wnan.1339]

[24]

Jarrett BR, Frendo M, Vogan J, Louie AY. Size-controlled synthesis of dextran sulfate coated iron oxide nanoparticles for magnetic resonance imaging. Nanotechnology 2007; 18(3): 035603. [PMID: 19636126 DOI: 10.1088/0957-4484/18/3/035603]

[25]

Iacob AT, Lupascu FG, Apotrosoaei M, Vasincu IM, Tauser RG, et al. Recent biomedical approaches for chitosan based materials as drug delivery nanocarriers. Pharmaceutics 2021; 13(4): 587. [PMID: 33924046 DOI: 10.3390/pharmaceutics13040587]

[26]

Yu M, Zheng J. Clearance pathways and tumor targeting of imaging nanoparticles. ACS Nano 2015; 9(7): 6655-74. [PMID: 26149184 DOI: 10.1021/acsnano.5b01320]

[27]

Yan J, Wu Q, Zhao Z, Wu J, Ye H, et al. Light-assisted hierarchical intratumoral penetration and programmed antitumor therapy based on tumor microenvironment (TME)-amendatory and self-adaptive polymeric nanoclusters. Biomaterials 2020; 255: 120166. [PMID: 32544718 DOI: 10.1016/j.biomaterials.2020.120166]

[28]

Li H-J, Du J-Z, Liu J, Du X-J, Shen S, et al. Smart superstructures with ultrahigh pH-sensitivity for targeting acidic tumor microenvironment: instantaneous size switching and improved tumor penetration. ACS Nano 2016; 10(7): 6753-61. [PMID: 27244096 DOI: 10.1021/acsnano.6b02326]

[29]

Liu X, Liu Z, Dong K, Wu S, Sang Y, et al. Tumor-activatable ultrasmall nanozyme generator for enhanced penetration and deep catalytic therapy. Biomaterials 2020; 258: 120263. [PMID: 32798740 DOI: 10.1016/j.biomaterials.2020.120263]

[30]

Liu Y, Lu Y, Zhu X, Li C, Yan M, et al. Tumor microenvironment-responsive prodrug nanoplatform via co-self-assembly of photothermal agent and IDO inhibitor for enhanced tumor penetration and cancer immunotherapy. Biomaterials 2020; 242: 119933. [PMID: 32151859 DOI: 10.1016/j.biomaterials.2020.119933]

[31]

Han M, Huang-Fu M-Y, Guo W-W, Guo N-N, Chen J, et al. MMP-2-Sensitive HA end-conjugated poly(amidoamine) dendrimers via click reaction to enhance drug penetration into solid tumor. ACS Appl Mater Interfaces 2017; 9(49): 42459-70. [PMID: 29143522 DOI: 10.1021/acsami.7b10098]

[32]

Huang J, Xian S, Liu Y, Chen X, Pu K, et al. A renally clearable activatable polymeric nanoprobe for early detection of hepatic ischemia-reperfusion injury. Adv Mater 2022; 34(24): e2201357. [PMID: 35436014 DOI: 10.1002/adma.202201357]

[33]

Ruan B, Yu M, Zhou Y, Xu W, Liu Y, et al. Size-transformable superoxide-triggered nanoreporters for crosstalk-free dual fluorescence/chemiluminescence imaging and urinalysis in living mice. Angew Chem Int Ed Engl 2023; 62(31): e202305812. [PMID: 37258940 DOI: 10.1002/anie.202305812]

[34]

De Jong WH, Hagens WI, Krystek P, Burger MC, Sips AJAM, et al. Particle size-dependent organ distribution of gold nanoparticles after intravenous administration. Biomaterials 2008; 29(12): 1912-9. [PMID: 18242692 DOI: 10.1016/j.biomaterials.2007.12.037]

[35]

Yang Y, Yang T, Chen F, Zhang C, Yin B, et al. Degradable magnetic nanoplatform with hydroxide ions triggered photoacoustic, MR imaging, and photothermal conversion for precise cancer theranostic. Nano Lett 2022; 22(8): 3228-35. [PMID: 35380847 DOI: 10.1021/acs.nanolett.1c04804]

[36]

Hwang J, Jeong Y, Park JM, Lee KH, Hong JW, et al. Biomimetics: forecasting the future of science, engineering, and medicine. Int J Nanomedicine 2015; 10: 5701-13. [PMID: 26388692 DOI: 10.2147/IJN.S83642]

[37]

Kroll AV, Fang RH, Zhang L. Biointerfacing and applications of cell membrane-coated nanoparticles. Bioconjug Chem 2017; 28(1): 23-32. [PMID: 27798829 DOI: 10.1021/acs.bioconjchem.6b00569]

[38]

Peng P, Hu J. [Erythrocytes-camouflaged nanoparticles: a promising delivery system for drugs and vaccines]. Sheng Wu Gong Cheng Xue Bao 2023; 39(1): 159-76. [PMID: 36738208 DOI: 10.13345/j.cjb.220166]

[39]

Pasto A, Giordano F, Evangelopoulos M, Amadori A, Tasciotti E. Cell membrane protein functionalization of nanoparticles as a new tumor-targeting strategy. Clin Transl Med 2019; 8(1): 8. [PMID: 30877412 DOI: 10.1186/s40169-019-0224-y]

[40]

Rao L, Bu L-L, Xu J-H, Cai B, Yu G-T, et al. Red blood cell membrane as a biomimetic nanocoating for prolonged circulation time and reduced accelerated blood clearance. Small 2015; 11(46): 6225-36. [PMID: 26488923 DOI: 10.1002/smll.201502388]

[41]

Wei X, Gao J, Fang RH, Luk BT, Kroll AV, et al. Nanoparticles camouflaged in platelet membrane coating as an antibody decoy for the treatment of immune thrombocytopenia. Biomaterials 2016; 111: 116-23. [PMID: 27728811 DOI: 10.1016/j.biomaterials.2016.10.003]

[42]

Xu C-H, Ye P-J, Zhou Y-C, He D-X, Wei H, et al. Cell membrane-camouflaged nanoparticles as drug carriers for cancer therapy. Acta Biomater 2020; 105: 1-14. [PMID: 32001369 DOI: 10.1016/j.actbio.2020.01.036]

[43]

Choi MJ, Lee YK, Choi KC, Lee DH, Jeong HY, et al. Tumor-targeted erythrocyte membrane nanoparticles for theranostics of triple-negative breast cancer. Pharmaceutics 2023; 15(2): 350. [PMID: 36839675 DOI: 10.3390/pharmaceutics15020350]

[44]

Li B, Wang F, Gui L, He Q, Yao Y, et al. The potential of biomimetic nanoparticles for tumor-targeted drug delivery. Nanomedicine (Lond) 2018; 13(16): 2099-118. [PMID: 30226404 DOI: 10.2217/nnm-2018-0017]

[45]

Chen Y, Zhao G, Wang S, He Y, Han S, et al. Platelet-membrane-camouflaged bismuth sulfide nanorods for synergistic radio-photothermal therapy against cancer. Biomater Sci 2019; 7(8): 3450-9. [PMID: 31268067 DOI: 10.1039/c9bm00599d]

[46]

Liu Y, Luo J, Chen X, Liu W, Chen T. Cell membrane coating technology: a promising strategy for biomedical applications. Nanomicro Lett 2019; 11(1): 100. [PMID: 34138027 DOI: 10.1007/s40820-019-0330-9]

[47]

Gao C, Wu Z, Lin Z, Lin X, He Q. Polymeric capsule-cushioned leukocyte cell membrane vesicles as a biomimetic delivery platform. Nanoscale 2016; 8(6): 3548-54. [PMID: 26804725 DOI: 10.1039/c5nr08407e]

[48]

Chen C, Song M, Du Y, Yu Y, Li C, et al. Tumor-associated-macrophage-membrane-coated nanoparticles for improved photodynamic immunotherapy. Nano Lett 2021; 21(13): 5522-31. [PMID: 34133181 DOI: 10.1021/acs.nanolett.1c00818]

[49]

Zhen X, Cheng P, Pu K. Recent advances in cell membrane-camouflaged nanoparticles for cancer phototherapy. Small 2019; 15(1): e1804105. [PMID: 30457701 DOI: 10.1002/smll.201804105]

[50]

Leibacher J, Henschler R. Biodistribution, migration and homing of systemically applied mesenchymal stem/stromal cells. Stem Cell Res Ther 2016; 7: 7. [PMID: 26753925 DOI: 10.1186/s13287-015-0271-2]

[51]

Timaner M, Letko-Khait N, Kotsofruk R, Benguigui M, Beyar-Katz O, et al. Therapy-educated mesenchymal stem cells enrich for tumor-initiating cells. Cancer Res 2018; 78(5): 1253-65. [PMID: 29301792 DOI: 10.1158/0008-5472.CAN-17-1547]

[52]

Rao L, Bu L-L, Cai B, Xu J-H, Li A, et al. Cancer cell membrane-coated upconversion nanoprobes for highly specific tumor imaging. Adv Mater 2016; 28(18): 3460-6. [PMID: 26970518 DOI: 10.1002/adma.201506086]

[53]

Chen Z, Zhao P, Luo Z, Zheng M, Tian H, et al. Cancer cell membrane-biomimetic nanoparticles for homologous-targeting dual-modal imaging and photothermal therapy. ACS Nano 2016; 10(11): 10049-57. [PMID: 27934074 DOI: 10.1021/acsnano.6b04695]

[54]

Fang RH, Hu C-M, Chen KNH, Luk BT, Carpenter CW, et al. Lipid-insertion enables targeting functionalization of erythrocyte membrane-cloaked nanoparticles. Nanoscale 2013; 5(19): 8884-8. [PMID: 23907698 DOI: 10.1039/c3nr03064d]

[55]

Dehaini D, Wei X, Fang RH, Masson S, Angsantikul P, et al. Erythrocyte-platelet hybrid membrane coating for enhanced nanoparticle functionalization. Adv Mater 2017; 29(16): 1606209. [PMID: 28199033 DOI: 10.1002/adma.201606209]

[56]

Chugh V, Vijaya Krishna K, Pandit A. Cell membrane-coated mimics: a methodological approach for fabrication, characterization for therapeutic applications, and challenges for clinical translation. ACS Nano 2021; 15(11): 17080-123. [PMID: 34699181 DOI: 10.1021/acsnano.1c03800]

[57]

Zeng Y, Li S, Zhang S, Wang L, Yuan H, et al. Cell membrane coated-nanoparticles for cancer immunotherapy. Acta Pharm Sin B 2022; 12(8): 3233-54. [PMID: 35967284 DOI: 10.1016/j.apsb.2022.02.023]

[58]

Gangadaran P, Hong CM, Ahn B-C. An update on in vivo imaging of extracellular vesicles as drug delivery vehicles. Front Pharmacol 2018; 9: 169. [PMID: 29541030 DOI: 10.3389/fphar.2018.00169]

[59]

Jia S, Zocco D, Samuels ML, Chou MF, Chammas R, et al. Emerging technologies in extracellular vesicle-based molecular diagnostics. Expert Rev Mol Diagn 2014; 14(3): 307-21. [PMID: 24575799 DOI: 10.1586/14737159.2014.893828]

[60]

Vlassov AV, Magdaleno S, Setterquist R, Conrad R. Exosomes: current knowledge of their composition, biological functions, and diagnostic and therapeutic potentials. Biochim Biophys Acta 2012; 1820(7): 940-8. [PMID: 22503788 DOI: 10.1016/j.bbagen.2012.03.017]

[61]

Nolte-’t Hoen E, Cremer T, Gallo RC, Margolis LB. Extracellular vesicles and viruses: are they close relatives? Proc Natl Acad Sci U S A 2016; 113(33): 9155-61. [PMID: 27432966 DOI: 10.1073/pnas.1605146113]

[62]

Escrevente C, Keller S, Altevogt P, Costa J. Interaction and uptake of exosomes by ovarian cancer cells. BMC Cancer 2011; 11: 108. [PMID: 21439085 DOI: 10.1186/1471-2407-11-108]

[63]

Kalimuthu S, Gangadaran P, Li XJ, Oh JM, Lee HW, et al. In Vivo therapeutic potential of mesenchymal stem cell-derived extracellular vesicles with optical imaging reporter in tumor mice model. Sci Rep 2016; 6: 30418. [PMID: 27452924 DOI: 10.1038/srep30418]

[64]

Gangadaran P, Rajendran RL, Lee HW, Kalimuthu S, Hong CM, et al. Extracellular vesicles from mesenchymal stem cells activates VEGF receptors and accelerates recovery of hindlimb ischemia. J Control Release 2017; 264: 112-26. [PMID: 28837823 DOI: 10.1016/j.jconrel.2017.08.022]

[65]

Bunggulawa EJ, Wang W, Yin T, Wang N, Durkan C, et al. Recent advancements in the use of exosomes as drug delivery systems. J Nanobiotechnology 2018; 16(1): 81. [PMID: 30326899 DOI: 10.1186/s12951-018-0403-9]

[66]

Li X, Tsibouklis J, Weng T, Zhang B, Yin G, et al. Nano carriers for drug transport across the blood-brain barrier. J Drug Target 2017; 25(1): 17-28. [PMID: 27126681 DOI: 10.1080/1061186X.2016.1184272]

[67]

Kim H, Jang H, Cho H, Choi J, Hwang KY, et al. Recent advances in exosome-based drug delivery for cancer therapy. Cancers (Basel) 2021; 13(17): 4435. [PMID: 34503245 DOI: 10.3390/cancers13174435]

[68]

Kim H, Kim EH, Kwak G, Chi S-G, Kim SH, et al. Exosomes: cell-derived nanoplatforms for the delivery of cancer therapeutics. Int J Mol Sci 2020; 22(1): 14. [PMID: 33374978 DOI: 10.3390/ijms22010014]

[69]

Hoshino A, Costa-Silva B, Shen T-L, Rodrigues G, Hashimoto A, et al. Tumour exosome integrins determine organotropic metastasis. Nature 2015; 527(7578): 329-35. [PMID: 26524530 DOI: 10.1038/nature15756]

[70]

Frontiers Editorial Office . Retraction: targeting and therapy of glioblastoma in a mouse model using exosomes derived from natural killer cells. Front Immunol 2019; 10: 1770. [PMID: 31379887 DOI: 10.3389/fimmu.2019.01770]

[71]

Qian R, Jing B, Jiang D, Gai Y, Zhu Z, et al. Multi-antitumor therapy and synchronous imaging monitoring based on exosome. Eur J Nucl Med Mol Imaging 2022; 49(8): 2668-81. [PMID: 35091755 DOI: 10.1007/s00259-022-05696-x]

[72]

Kimiz-Gebologlu I, Oncel SS. Exosomes: large-scale production, isolation, drug loading efficiency, and biodistribution and uptake. J Control Release 2022; 347: 533-43. [PMID: 35597405 DOI: 10.1016/j.jconrel.2022.05.027]

[73]

Ming-Kun C, Zi-Xian C, Mao-Ping C, Hong C, Zhuang-Fei C, et al. Engineered extracellular vesicles: a new approach for targeted therapy of tumors and overcoming drug resistance. Cancer Commun (Lond) 2024; 44(2): 205-25. [PMID: 38155418 DOI: 10.1002/cac2.12518]

[74]

Yang D, Zhang W, Zhang H, Zhang F, Chen L, et al. Progress, opportunity, and perspective on exosome isolation - efforts for efficient exosome-based theranostics. Theranostics 2020; 10(8): 3684-707. [PMID: 32206116 DOI: 10.7150/thno.41580]

[75]

Shen J, Ma Z, Xu J, Xue T, Lv X, et al. Exosome isolation and detection: from microfluidic chips to nanoplasmonic biosensor. ACS Appl Mater Interfaces 2024; 16(18): 22776-93. [PMID: 38676635 DOI: 10.1021/acsami.3c19396]

[76]

Jeong S, Park J, Pathania D, Castro CM, Weissleder R, et al. Integrated magneto-electrochemical sensor for exosome analysis. ACS Nano 2016; 10(2): 1802-9. [PMID: 26808216 DOI: 10.1021/acsnano.5b07584]

[77]

Li Y, Ma X, Yue Y, Zhang K, Cheng K, et al. Rapid surface display of mRNA antigens by bacteria-derived outer membrane vesicles for a personalized tumor vaccine. Adv Mater 2022; 34(20): e2109984. [PMID: 35315546 DOI: 10.1002/adma.202109984]

[78]

Li M, Zhou H, Yang C, Wu Y, Zhou X, et al. Bacterial outer membrane vesicles as a platform for biomedical applications: an update. J Control Release 2020; 323: 253-68. [PMID: 32333919 DOI: 10.1016/j.jconrel.2020.04.031]

[79]

Xie J, Li Q, Haesebrouck F, Van Hoecke L, Vandenbroucke RE. The tremendous biomedical potential of bacterial extracellular vesicles. Trends Biotechnol 2022; 40(10): 1173-94. [PMID: 35581020 DOI: 10.1016/j.tibtech.2022.03.005]

[80]

Kaparakis-Liaskos M, Ferrero RL. Immune modulation by bacterial outer membrane vesicles. Nat Rev Immunol 2015; 15(6): 375-87. [PMID: 25976515 DOI: 10.1038/nri3837]

[81]

Li M, Li S, Zhou H, Tang X, Wu Y, et al. Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy. Nat Commun 2020; 11(1): 1126. [PMID: 32111847 DOI: 10.1038/s41467-020-14963-0]

[82]

Chen Q, Rozovsky S, Chen W. Engineering multi-functional bacterial outer membrane vesicles as modular nanodevices for biosensing and bioimaging. Chem Commun (Camb) 2017; 53(54): 7569-72. [PMID: 28636010 DOI: 10.1039/c7cc04246a]

[83]

Kim OY, Park HT, Dinh NTH, Choi SJ, Lee J, et al. Bacterial outer membrane vesicles suppress tumor by interferon-γ-mediated antitumor response. Nat Commun 2017; 8(1): 626. [PMID: 28931823 DOI: 10.1038/s41467-017-00729-8]

[84]

Xiang S, Khan A, Yao Q, Wang D. Recent advances in bacterial outer membrane vesicles: Effects on the immune system, mechanisms and their usage for tumor treatment. J Pharm Anal 2024; 14(12): 101049. [PMID: 39840399 DOI: 10.1016/j.jpha.2024.101049]

[85]

Wang X, Quinn PJ. Lipopolysaccharide: biosynthetic pathway and structure modification. Prog Lipid Res 2010; 49(2): 97-107. [PMID: 19815028 DOI: 10.1016/j.plipres.2009.06.002]

[86]

Collins SM, Brown AC. Bacterial outer membrane vesicles as antibiotic delivery vehicles. Front Immunol 2021; 12: 733064. [PMID: 34616401 DOI: 10.3389/fimmu.2021.733064]

[87]

Needham BD, Carroll SM, Giles DK, Georgiou G, Whiteley M, et al. Modulating the innate immune response by combinatorial engineering of endotoxin. Proc Natl Acad Sci U S A 2013; 110(4): 1464-9. [PMID: 23297218 DOI: 10.1073/pnas.1218080110]

[88]

Zhu Z, Antenucci F, Villumsen KR, Bojesen AM. Bacterial outer membrane vesicles as a versatile tool in vaccine research and the fight against antimicrobial resistance. mBio 2021; 12(4): e0170721. [PMID: 34372691 DOI: 10.1128/mBio.01707-21]

[89]

Orench-Rivera N, Kuehn MJ. Environmentally controlled bacterial vesicle-mediated export. Cell Microbiol 2016; 18(11): 1525-36. [PMID: 27673272 DOI: 10.1111/cmi.12676]

[90]

Prados-Rosales R, Weinrick BC, Piqué DG, Jacobs WR Jr, Casadevall A, et al. Role for Mycobacterium tuberculosis membrane vesicles in iron acquisition. J Bacteriol 2014; 196(6): 1250-6. [PMID: 24415729 DOI: 10.1128/JB.01090-13]

[91]

Keenan JI, Allardyce RA. Iron influences the expression of Helicobacter pylori outer membrane vesicle-associated virulence factors. Eur J Gastroenterol Hepatol 2000; 12(12): 1267-73. [PMID: 11192314 DOI: 10.1097/00042737-200012120-00002]

[92]

Toyofuku M, Zhou S, Sawada I, Takaya N, Uchiyama H, et al. Membrane vesicle formation is associated with pyocin production under denitrifying conditions in Pseudomonas aeruginosa PAO1. Environ Microbiol 2014; 16(9): 2927-38. [PMID: 24112564 DOI: 10.1111/1462-2920.12260]

[93]

Zariri A, Beskers J, van de Waterbeemd B, Hamstra HJ, Bindels THE, et al. Meningococcal outer membrane vesicle composition-dependent activation of the innate immune response. Infect Immun 2016; 84(10): 3024-33. [PMID: 27481244 DOI: 10.1128/IAI.00635-16]

[94]

Macdonald IA, Kuehn MJ. Stress-induced outer membrane vesicle production by Pseudomonas aeruginosa. J Bacteriol 2013; 195(13): 2971-81. [PMID: 23625841 DOI: 10.1128/JB.02267-12]

[95]

van de Waterbeemd B, Zomer G, van den Ijssel J, van Keulen L, Eppink MH, et al. Cysteine depletion causes oxidative stress and triggers outer membrane vesicle release by Neisseria meningitidis; implications for vaccine development. PLoS One 2013; 8(1): e54314. [PMID: 23372704 DOI: 10.1371/journal.pone.0054314]

[96]

Bernadac A, Gavioli M, Lazzaroni JC, Raina S, Lloubès R. Escherichia coli tol-pal mutants form outer membrane vesicles. J Bacteriol 1998; 180(18): 4872-8. [PMID: 9733690 DOI: 10.1128/JB.180.18.4872-4878.1998]

[97]

Szczepaniak J, Press C, Kleanthous C. The multifarious roles of Tol-Pal in Gram-negative bacteria. FEMS Microbiol Rev 2020; 44(4): 490-506. [PMID: 32472934 DOI: 10.1093/femsre/fuaa018]

[98]

Luzio JP, Pryor PR, Bright NA. Lysosomes: fusion and function. Nat Rev Mol Cell Biol 2007; 8(8): 622-32. [PMID: 17637737 DOI: 10.1038/nrm2217]

[99]

Gujrati V, Lee M, Ko Y-J, Lee S, Kim D, et al. Bioengineered yeast-derived vacuoles with enhanced tissue-penetrating ability for targeted cancer therapy. Proc Natl Acad Sci U S A 2016; 113(3): 710-5. [PMID: 26715758 DOI: 10.1073/pnas.1509371113]

[100]

Armstrong J. Yeast vacuoles: more than a model lysosome. Trends Cell Biol 2010; 20(10): 580-5. [PMID: 20685121 DOI: 10.1016/j.tcb.2010.06.010]

[101]

Nguyen N-H, Nguyen N-T, Kim YH, Min J. Yeast-derived vacuoles as a novel carrier with enhanced hCMEC/D3 cell monolayer penetration. Biotechnol J 2023; 18(2): e2200393. [PMID: 36321515 DOI: 10.1002/biot.202200393]

[102]

Wickner W. Yeast vacuoles and membrane fusion pathways. EMBO J 2002; 21(6): 1241-7. [PMID: 11889030 DOI: 10.1093/emboj/21.6.1241]

[103]

Zieger M, Mayer A. Yeast vacuoles fragment in an asymmetrical two-phase process with distinct protein requirements. Mol Biol Cell 2012; 23(17): 3438-49. [PMID: 22787281 DOI: 10.1091/mbc.E12-05-0347]

[104]

Choi W, Shin W-R, Kim Y-H, Min J. Inducing a proinflammatory response with bioengineered yeast vacuoles with TLR2-binding peptides (VacT2BP) as a drug carrier for daunorubicin delivery. ACS Appl Mater Interfaces 2023; 15(35): 41258-70. [PMID: 37615983 DOI: 10.1021/acsami.3c06669]

[105]

Nevoigt E. Progress in metabolic engineering of Saccharomyces cerevisiae. Microbiol Mol Biol Rev 2008; 72(3): 379-412. [PMID: 18772282 DOI: 10.1128/MMBR.00025-07]

[106]

Liang Y, Duan L, Lu J, Xia J. Engineering exosomes for targeted drug delivery. Theranostics 2021; 11(7): 3183-95. [PMID: 33537081 DOI: 10.7150/thno.52570]

[107]

Boudna M, Campos AD, Vychytilova-Faltejskova P, Machackova T, Slaby O, et al. Strategies for labelling of exogenous and endogenous extracellular vesicles and their application for in vitro and in vivo functional studies. Cell Commun Signal 2024; 22(1): 171. [PMID: 38461237 DOI: 10.1186/s12964-024-01548-3]

[108]

Vader P, Mol EA, Pasterkamp G, Schiffelers RM. Extracellular vesicles for drug delivery. Adv Drug Deliv Rev 2016; 106(Pt A): 148-56. [PMID: 26928656 DOI: 10.1016/j.addr.2016.02.006]

[109]

Anas A, Okuda T, Kawashima N, Nakayama K, Itoh T, et al. Clathrin-mediated endocytosis of quantum dot-peptide conjugates in living cells. ACS Nano 2009; 3(8): 2419-29. [PMID: 19653641 DOI: 10.1021/nn900663r]

[110]

Wang Z, Mo H, He Z, Chen A, Cheng P. Extracellular vesicles as an emerging drug delivery system for cancer treatment: Current strategies and recent advances. Biomed Pharmacother 2022; 153: 113480. [PMID: 36076581 DOI: 10.1016/j.biopha.2022.113480]

[111]

Jiang A, Nie W, Xie H-Y. In vivo imaging for the visualization of extracellular vesicle-based tumor therapy. ChemistryOpen 2022; 11(9): e202200124. [PMID: 36101512 DOI: 10.1002/open.202200124]

[112]

Jing B, Qian R, Jiang D, Gai Y, Liu Z, et al. Extracellular vesicles-based pre-targeting strategy enables multi-modal imaging of orthotopic colon cancer and image-guided surgery. J Nanobiotechnology 2021; 19(1): 151. [PMID: 34022897 DOI: 10.1186/s12951-021-00888-3]

[113]

Sun J-X, Xu J-Z, An Y, Ma S-Y, Liu C-Q, et al. Future in precise surgery: fluorescence-guided surgery using EVs derived fluorescence contrast agent. J Control Release 2023; 353: 832-41. [PMID: 36496053 DOI: 10.1016/j.jconrel.2022.12.013]

[114]

Han Z, Liu S, Pei Y, Ding Z, Li Y, et al. Highly efficient magnetic labelling allows MRI tracking of the homing of stem cell-derived extracellular vesicles following systemic delivery. J Extracell Vesicles 2021; 10(3): e12054. [PMID: 33489014 DOI: 10.1002/jev2.12054]

[115]

Yang Y, Zhang F. Molecular fluorophores for in vivo bioimaging in the second near-infrared window. Eur J Nucl Med Mol Imaging 2022; 49(9): 3226-46. [PMID: 35088125 DOI: 10.1007/s00259-022-05688-x]

[116]

Duan Y, Liu B. Recent advances of optical imaging in the second near-infrared window. Adv Mater 2018; 30(47): e1802394. [PMID: 30182451 DOI: 10.1002/adma.201802394]

[117]

Su Y, Yu B, Wang S, Cong H, Shen Y. NIR-II bioimaging of small organic molecule. Biomaterials 2021; 271: 120717. [PMID: 33610960 DOI: 10.1016/j.biomaterials.2021.120717]

[118]

Hong G, Diao S, Antaris AL, Dai H. Carbon nanomaterials for biological imaging and nanomedicinal therapy. Chem Rev 2015; 115(19): 10816-906. [PMID: 25997028 DOI: 10.1021/acs.chemrev.5b00008]

[119]

Shiraki T, Miyauchi Y, Matsuda K, Nakashima N. Carbon nanotube photoluminescence modulation by local chemical and supramolecular chemical functionalization. Acc Chem Res 2020; 53(9): 1846-59. [PMID: 32791829 DOI: 10.1021/acs.accounts.0c00294]

[120]

Bruns OT, Bischof TS, Harris DK, Franke D, Shi Y, et al. Next-generation in vivo optical imaging with short-wave infrared quantum dots. Nat Biomed Eng 2017; 1: 0056. [PMID: 29119058 DOI: 10.1038/s41551-017-0056]

[121]

Li X, Zha M, Li Y, Ni J-S, Min T, et al. Sub-10 nm aggregation-induced emission quantum dots assembled by microfluidics for enhanced tumor targeting and reduced retention in the liver. Angew Chem Int Ed Engl 2020; 59(49): 21899-903. [PMID: 32841464 DOI: 10.1002/anie.202008564]

[122]

Wang R, Zhou L, Wang W, Li X, Zhang F. In vivo gastrointestinal drug-release monitoring through second near-infrared window fluorescent bioimaging with orally delivered microcarriers. Nat Commun 2017; 8: 14702. [PMID: 28281530 DOI: 10.1038/ncomms14702]

[123]

He S, Chen S, Li D, Wu Y, Zhang X, et al. High affinity to skeleton rare earth doped nanoparticles for near-infrared II imaging. Nano Lett 2019; 19(5): 2985-92. [PMID: 30983358 DOI: 10.1021/acs.nanolett.9b00140]

[124]

Hemmateenejad B, Shamsipur M, Khosousi T, Shanehsaz M, Firuzi O. Antioxidant activity assay based on the inhibition of oxidation and photobleaching of L-cysteine-capped CdTe quantum dots. Analyst 2012; 137(17): 4029-36. [PMID: 22814421 DOI: 10.1039/c2an35588d]

[125]

Shamsipur M, Rajabi HR. Pure zinc sulfide quantum dot as highly selective luminescent probe for determination of hazardous cyanide ion. Mater Sci Eng C Mater Biol Appl 2014; 36: 139-45. [PMID: 24433896 DOI: 10.1016/j.msec.2013.12.001]

[126]

Xu Z, Huang H, Xiong X, Wei X, Guo X, et al. A near-infrared light-responsive extracellular vesicle as a “Trojan horse” for tumor deep penetration and imaging-guided therapy. Biomaterials 2021; 269: 120647. [PMID: 33450584 DOI: 10.1016/j.biomaterials.2020.120647]

[127]

Chen L-L, Zhao L, Wang Z-G, Liu S-L, Pang D-W. Near-infrared-II quantum dots for in vivo imaging and cancer therapy. Small 2022; 18(8): e2104567. [PMID: 34837314 DOI: 10.1002/smll.202104567]

[128]

Liu A-A, Cui R, Zong X, Jia J, Hu Y, et al. Live-cell synthesis of biocompatible quantum dots. Nat Protoc 2025; 20(7): 1884-914. [PMID: 40097832 DOI: 10.1038/s41596-024-01133-5]

[129]

Zhou J, Yang Y, Zhang CY. Toward biocompatible semiconductor quantum dots: from biosynthesis and bioconjugation to biomedical application. Chem Rev 2015; 115(21): 11669-717. [PMID: 26446443 DOI: 10.1021/acs.chemrev.5b00049]

[130]

Liu A-A, Sun E-Z, Wang Z-G, Liu S-L, Pang D-W. Artificially regulated synthesis of nanocrystals in live cells. Natl Sci Rev 2021; 9(6): nwab162. [PMID: 35874310 DOI: 10.1093/nsr/nwab162]

[131]

Hong Z-Y, Liu H-M, Yu Z-L, Chen G, Wu M. Nanometer-sized and near-infrared-II fluorescent extracellular vesicles for noninvasive high-contrast imaging of tumors with high EGFR expression. ACS Appl Nano Mater 2023; 6(13): 11481-90. [DOI: 10.1021/acsanm.3c01527]

[132]

Li S, Ruan Z, Zhang H, Xu H. Recent achievements of bioluminescence imaging based on firefly luciferin-luciferase system. Eur J Med Chem 2021; 211: 113111. [PMID: 33360804 DOI: 10.1016/j.ejmech.2020.113111]

[133]

England CG, Ehlerding EB, Cai W. NanoLuc: a small luciferase is brightening up the field of bioluminescence. Bioconjug Chem 2016; 27(5): 1175-87. [PMID: 27045664 DOI: 10.1021/acs.bioconjchem.6b00112]

[134]

Coralli C, Cemazar M, Kanthou C, Tozer GM, Dachs GU. Limitations of the reporter green fluorescent protein under simulated tumor conditions. Cancer Res 2001; 61(12): 4784-90. [PMID: 11406553]

[135]

Contag CH, Bachmann MH. Advances in in vivo bioluminescence imaging of gene expression. Annu Rev Biomed Eng 2002; 4: 235-60. [PMID: 12117758 DOI: 10.1146/annurev.bioeng.4.111901.093336]

[136]

Welsh DK, Noguchi T. Cellular bioluminescence imaging. Cold Spring Harb Protoc 2012; 2012(8): pdb.top070607. [PMID: 22854570 DOI: 10.1101/pdb.top070607]

[137]

Harris DA, Patel SH, Gucek M, Hendrix A, Westbroek W, et al. Exosomes released from breast cancer carcinomas stimulate cell movement. PLoS One 2015; 10(3): e0117495. [PMID: 25798887 DOI: 10.1371/journal.pone.0117495]

[138]

Setti M, Osti D, Richichi C, Ortensi B, Del Bene M, et al. Extracellular vesicle-mediated transfer of CLIC1 protein is a novel mechanism for the regulation of glioblastoma growth. Oncotarget 2015; 6(31): 31413-27. [PMID: 26429879 DOI: 10.18632/oncotarget.5105]

[139]

Rodríguez M, Silva J, Herrera A, Herrera M, Peña C, et al. Exosomes enriched in stemness/metastatic-related mRNAS promote oncogenic potential in breast cancer. Oncotarget 2015; 6(38): 40575-87. [PMID: 26528758 DOI: 10.18632/oncotarget.5818]

[140]

Hood JL, San RS, Wickline SA. Exosomes released by melanoma cells prepare sentinel lymph nodes for tumor metastasis. Cancer Res 2011; 71(11): 3792-801. [PMID: 21478294 DOI: 10.1158/0008-5472.CAN-10-4455]

[141]

Gangadaran P, Li XJ, Lee HW, Oh JM, Kalimuthu S, et al. A new bioluminescent reporter system to study the biodistribution of systematically injected tumor-derived bioluminescent extracellular vesicles in mice. Oncotarget 2017; 8(66): 109894-914. [PMID: 29299117 DOI: 10.18632/oncotarget.22493]

[142]

Hikita T, Miyata M, Watanabe R, Oneyama C. Sensitive and rapid quantification of exosomes by fusing luciferase to exosome marker proteins. Sci Rep 2018; 8(1): 14035. [PMID: 30232365 DOI: 10.1038/s41598-018-32535-7]

[143]

Huang Y, Beringhs AO, Chen Q, Song D, Chen W, et al. Genetically engineered bacterial outer membrane vesicles with expressed nanoluciferase reporter for in vivo bioluminescence kinetic modeling through noninvasive imaging. ACS Appl Bio Mater 2019; 2(12): 5608-15. [PMID: 35021555 DOI: 10.1021/acsabm.9b00690]

[144]

Zeng Y, Dou T, Ma L, Ma J. Biomedical photoacoustic imaging for molecular detection and disease diagnosis: “always-on” and “turn-on” probes. Adv Sci (Weinh) 2022; 9(25): e2202384. [PMID: 35773244 DOI: 10.1002/advs.202202384]

[145]

Jiang Y, Pu K. Advanced photoacoustic imaging applications of near-infrared absorbing organic nanoparticles. Small 2017; 13(30). [PMID: 28597608 DOI: 10.1002/smll.201700710]

[146]

Fu Q, Zhu R, Song J, Yang H, Chen X. Photoacoustic imaging: contrast agents and their biomedical applications. Adv Mater 2019; 31(6): e1805875. [PMID: 30556205 DOI: 10.1002/adma.201805875]

[147]

Chaudhary Z, Khan GM, Abeer MM, Pujara N, Wan-Chi Tse B, et al. Efficient photoacoustic imaging using indocyanine green (ICG) loaded functionalized mesoporous silica nanoparticles. Biomater Sci 2019; 7(12): 5002-15. [PMID: 31617526 DOI: 10.1039/c9bm00822e]

[148]

Li S, Jiang W, Yuan Y, Sui M, Yang Y, et al. Delicately designed cancer cell membrane-camouflaged nanoparticles for targeted 19F MR/PA/FL imaging-guided photothermal therapy. ACS Appl Mater Interfaces 2020; 12(51): 57290-301. [PMID: 33231083 DOI: 10.1021/acsami.0c13865]

[149]

Stritzker J, Kirscher L, Scadeng M, Deliolanis NC, Morscher S, et al. Vaccinia virus-mediated melanin production allows MR and optoacoustic deep tissue imaging and laser-induced thermotherapy of cancer. Proc Natl Acad Sci U S A 2013; 110(9): 3316-20. [PMID: 23401518 DOI: 10.1073/pnas.1216916110]

[150]

Fan Q, Cheng K, Hu X, Ma X, Zhang R, et al. Transferring biomarker into molecular probe: melanin nanoparticle as a naturally active platform for multimodality imaging. J Am Chem Soc 2014; 136(43): 15185-94. [PMID: 25292385 DOI: 10.1021/ja505412p]

[151]

Jang Y, Kim H, Yoon S, Lee H, Hwang J, et al. Exosome-based photoacoustic imaging guided photodynamic and immunotherapy for the treatment of pancreatic cancer. J Control Release 2021; 330: 293-304. [PMID: 33359580 DOI: 10.1016/j.jconrel.2020.12.039]

[152]

Lu Z-R, Laney V, Li Y. Targeted contrast agents for magnetic resonance molecular imaging of cancer. Acc Chem Res 2022; 55(19): 2833-47. [PMID: 36121350 DOI: 10.1021/acs.accounts.2c00346]

[153]

Sanvicens N, Marco MP. Multifunctional nanoparticles——properties and prospects for their use in human medicine. Trends Biotechnol 2008; 26(8): 425-33. [PMID: 18514941 DOI: 10.1016/j.tibtech.2008.04.005]

[154]

Hohnholt MC, Geppert M, Dringen R. Treatment with iron oxide nanoparticles induces ferritin synthesis but not oxidative stress in oligodendroglial cells. Acta Biomater 2011; 7(11): 3946-54. [PMID: 21763792 DOI: 10.1016/j.actbio.2011.06.052]

[155]

Du C, Liu X, Hu H, Li H, Yu L, et al. Dual-targeting and excretable ultrasmall SPIONs for T1-weighted positive MR imaging of intracranial glioblastoma cells by targeting the lipoprotein receptor-related protein. J Mater Chem B 2020; 8(11): 2296-306. [PMID: 32100784 DOI: 10.1039/c9tb02391g]

[156]

Rayamajhi S, Marasini R, Nguyen TDT, Plattner BL, Biller D, et al. Strategic reconstruction of macrophage-derived extracellular vesicles as a magnetic resonance imaging contrast agent. Biomater Sci 2020; 8(10): 2887-904. [PMID: 32300771 DOI: 10.1039/d0bm00128g]

[157]

Hu L, Wickline SA, Hood JL. Magnetic resonance imaging of melanoma exosomes in lymph nodes. Magn Reson Med 2015; 74(1): 266-71. [PMID: 25052384 DOI: 10.1002/mrm.25376]

[158]

Wang J, Zhu X, Li C, Cai L, Pei W, et al. Efficient EVs extraction through the conjugation of superparamagnetic iron oxide nanoparticles for the targeted delivery in rat brain. Mater Today Chem 2022; 23.

[159]

Kutchy NA, Ma R, Liu Y, Buch S, Hu G. Extracellular vesicle-mediated delivery of ultrasmall superparamagnetic iron oxide nanoparticles to mice brain. Front Pharmacol 2022; 13: 819516. [PMID: 35462907 DOI: 10.3389/fphar.2022.819516]

[160]

Wang J, Li W, Lu Z, Zhang L, Hu Y, et al. The use of RGD-engineered exosomes for enhanced targeting ability and synergistic therapy toward angiogenesis. Nanoscale 2017; 9(40): 15598-605. [PMID: 28990632 DOI: 10.1039/c7nr04425a]

[161]

Tian T, Zhang H-X, He C-P, Fan S, Zhu Y-L, et al. Surface functionalized exosomes as targeted drug delivery vehicles for cerebral ischemia therapy. Biomaterials 2018; 150: 137-49. [PMID: 29040874 DOI: 10.1016/j.biomaterials.2017.10.012]

[162]

Jia G, Han Y, An Y, Ding Y, He C, et al. NRP-1 targeted and cargo-loaded exosomes facilitate simultaneous imaging and therapy of glioma in vitro and in vivo. Biomaterials 2018; 178: 302-16. [PMID: 29982104 DOI: 10.1016/j.biomaterials.2018.06.029]

[163]

Chen L, Zhang G, Shi Y, Qiu R, Khan AA. Neuropilin-1 (NRP-1) and magnetic nanoparticles, a potential combination for diagnosis and therapy of gliomas. Curr Pharm Des 2015; 21(37): 5434-49. [PMID: 26377659 DOI: 10.2174/1381612821666150917092658]

[164]

Chen L, Miao W, Tang X, Zhang H, Wang S, et al. Inhibitory effect of neuropilin-1 monoclonal antibody (NRP-1 MAb) on glioma tumor in mice. J Biomed Nanotechnol 2013; 9(4): 551-8. [PMID: 23621013 DOI: 10.1166/jbn.2013.1623]

[165]

Galisova A, Zahradnik J, Allouche-Arnon H, Morandi MI, Abou Karam P, et al. Genetically engineered MRI-trackable extracellular vesicles as SARS-CoV-2 mimetics for mapping ACE2 binding in vivo. ACS Nano 2022; 16(8): 12276-89. [PMID: 35921522 DOI: 10.1021/acsnano.2c03119]

[166]

Lüdtke-Buzug K, Haegele J, Biederer S, Sattel TF, Erbe M, et al. Comparison of commercial iron oxide-based MRI contrast agents with synthesized high-performance MPI tracers. Biomed Tech (Berl) 2013; 58(6): 527-33. [PMID: 23787462 DOI: 10.1515/bmt-2012-0059]

[167]

Bulte JWM. Superparamagnetic iron oxides as MPI tracers: a primer and review of early applications. Adv Drug Deliv Rev 2019; 138: 293-301. [PMID: 30552918 DOI: 10.1016/j.addr.2018.12.007]

[168]

Capuzzo AM, Piccolantonio G, Negri A, Bontempi P, Lacavalla MA, et al. Comparison between USPIOs and SPIOs for multimodal imaging of extracellular vesicles extracted from adipose tissue-derived adult stem cells. Int J Mol Sci 2024; 25(17): 9701. [PMID: 39273647 DOI: 10.3390/ijms25179701]

[169]

Awanye AM, Chang C-M, Wheeler JX, Chan H, Marsay L, et al. Immunogenicity profiling of protein antigens from capsular group B Neisseria meningitidis. Sci Rep 2019; 9(1): 6843. [PMID: 31048732 DOI: 10.1038/s41598-019-43139-0]

[170]

Rollier CS, Dold C, Marsay L, Linder A, Green CA, et al. Human B cell responses to dominant and subdominant antigens induced by a meningococcal outer membrane vesicle vaccine in a phase I trial. mSphere 2022; 7(1): e0067421. [PMID: 35080470 DOI: 10.1128/msphere.00674-21]

[171]

Witwer KW, Wolfram J. Extracellular vesicles versus synthetic nanoparticles for drug delivery. Nat Rev Mater 2021; 6(2): 103-6. [PMID: 36117545 DOI: 10.1038/s41578-020-00277-6]

[172]

Xia Y, Zhang J, Liu G, Wolfram J. Immunogenicity of extracellular vesicles. Adv Mater 2024; 36(33): e2403199. [PMID: 38932653 DOI: 10.1002/adma.202403199]

[173]

Liu H, Zhang H, Han Y, Hu Y, Geng Z, et al. Bacterial extracellular vesicles-based therapeutic strategies for bone and soft tissue tumors therapy. Theranostics 2022; 12(15): 6576-94. [PMID: 36185613 DOI: 10.7150/thno.78034]

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