Preparation and Evaluation of Dual Targeting Nanoparticles for Oral Cancer

Shanshan Wu , Fuliang Xiong , Xueqiong Zhang , Tong Qiu , Mingxiu Tang , Xiaojing Ye , Zhijun Chen , Gang Zhou

Journal of Wuhan University of Technology Materials Science Edition ›› 2020, Vol. 34 ›› Issue (6) : 1495 -1504.

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Journal of Wuhan University of Technology Materials Science Edition ›› 2020, Vol. 34 ›› Issue (6) : 1495 -1504. DOI: 10.1007/s11595-019-2218-4
Biomaterial

Preparation and Evaluation of Dual Targeting Nanoparticles for Oral Cancer

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Abstract

A dual-receptor targeting delivery system based on acid-cleavage hydrazone bond was developed in the study. The characters of CMCS-hyd-CUR-EGFR- mAb were identifed. The in vitro release studies revealed that this drug delivery system was acid-sensitive, and the self-assembled nanoparticles which were spherical. The in vitro results indicated that the dual-receptor targeting nanoparticles could be faster internalized into the Cal-27 cells via receptor-mediated endocytosis, which exhibited better antitumor activity than the one-receptor nanoparticles. The experimental results clearly reveal that CMCS-hyd-CUR-EGFR mAb provides a novel way for drug delivery in oral cancer treatment.

Keywords

hydrazone bond / dual-receptor targeting / self-assembly / nanoparticle

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Shanshan Wu, Fuliang Xiong, Xueqiong Zhang, Tong Qiu, Mingxiu Tang, Xiaojing Ye, Zhijun Chen, Gang Zhou. Preparation and Evaluation of Dual Targeting Nanoparticles for Oral Cancer. Journal of Wuhan University of Technology Materials Science Edition, 2020, 34(6): 1495-1504 DOI:10.1007/s11595-019-2218-4

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References

[1]

Chang PY, Peng SF, Lee CY, et al. Curcumin-loaded Nanoparticles Induce Apoptotic Cell Death Through Regulation of the Function of MDR1 and Reactive Oxygen Species in Cisplatin-resistant CAR Human Oral Cancer Cells[J]. International Journal of Oncology, 2013, 43(4): 1 141-1 150.

[2]

Cheng YSL, Rees T, Wright J. A Review of Research on Salivary Biomarkers for Oral Cancer Detection[J]. Clinical & Translational Medicine, 2014, 3(1): 1 544-1 553.

[3]

Zlotogorski A, Dayan A, Dayan D, et al. Nutraceuticals as New Treatment Approaches for Oral Cancer: II. Green Tea Extracts and Resveratrol[J]. Oral Oncology, 2013, 49(3): 187-191.

[4]

Bandi R. Nanotechnology: A Pharmacutical Approach[J]. World Journal of Pharmaceutical Research, 2017, 6: 779-790.

[5]

Li M, Ma Y, Ngadi MO. Binding of Curcumin to β-lactoglobulin and Its Effect on Antioxidant Characteristics of Curcumin[J]. Food Chemistry, 2013, 141(2): 1 504-1 511.

[6]

Chopra M, Jain R, Dewangan AK, et al. Design of Curcumin Loaded Polymeric Nanoparticles-Optimization, Formulation and Characterization[J]. Journal of Nanoscience & Nanotechnology, 2016, 16(9): 9 432-9 442.

[7]

Neetu S, Vishal R, Deeba Z, et al. Insulin Catalyzes the Curcumin-in-duced Wound Healing: Anin Vitromodel for Gingival Repair[J]. Indian Journal of Pharmacology, 2012, 44(4): 458-462.

[8]

Ahmad MZ, Alkahtani SA, Akhter S, et al. Progress in Nanotechnology-based drug Carrier in Designing of Curcumin Nanomedicines for Cancer Therapy: Current State-of-the-art[J]. Journal of Drug Targeting, 2016, 24(4): 273-284.

[9]

Khalil NM, Casa DM, Dalmolin LF, et al. Pharmacokinetics of Curcumin-loaded PLGA and PLGA-PEG Blend Nanoparticles After Oral Administration in Rats[J]. Colloids & Surfaces B Biointerfaces, 2013, 101(1): 353-360.

[10]

Gao Y, Wang C, Sun M, et al. In Vivo Evaluation of Curcumin Loaded Nanosuspensions by Oral Administration[J]. Journal of Biomedical Nanotechnology, 2012, 8(4): 659-668.

[11]

Zhang X, Li L, Li C, et al. Cisplatin-crosslinked Glutathione-sensitive Micelles Loaded with Doxorubicin for Combination and Targeted Therapy of Tumors[J]. Carbohydrate Polymers, 2017, 155(2): 407-415.

[12]

Kayat J, Mehra NK, Gajbhiye V, et al. Drug Targeting to Arthritic Region Via Folic Acid Appended Surface-engineered Multi-walled Carbon Nanotubes[J]. Journal of Drug Targeting, 2015, 24(4): 318-327.

[13]

Cohen RB. Current Challenges and Clinical Investigations of Epidermal Growth Factor Receptor (EGFR) and ErbB Family-targeted Agents in the Treatment of Head and Neck Squamous Cell Carcinoma (HNSCC)[J]. Cancer Treatment Reviews, 2014, 40(4): 567-577.

[14]

Leemans CR, Braakhuis BJ, Brakenhoff RH. The Molecular Biology of Head and Neck Cancer[J]. Nature Reviews Cancer, 2011, 11(1): 9-22.

[15]

Jayakumar R, Prabaharan M, Nair SV, et al. Novel Carboxymethyl Derivatives of Chitin and Chitosan Materials and Their Biomedical Applications[J]. Progress in Materials Science, 2010, 55(7): 675-709.

[16]

Kaur S, Dhillon GS. The Versatile Biopolymer Chitosan: Potential Sources, Evaluation of Extraction Methods and Applications[J]. Critical Reviews in Microbiology, 2013, 40(2): 155-175.

[17]

Zhang X, Zhang H, Yin L, et al. A pH-Sensitive Nanosystem Based on Carboxymethyl Chitosan for Tumor-Targeted Delivery of Daunorubicin.[J]. Journal of Biomedical Nanotechnology, 2016, 12(8): 1 688-1 698.

[18]

Fu D, Han B, Dong W, et al. Effects of Carboxymethyl Chitosan on the Blood System of Rats[J]. Biochemical & Biophysical Research Communications, 2011, 408(1): 110-114.

[19]

Dong W, Han B, Feng Y, et al. Pharmacokinetics and Biodegradation Mechanisms of a Versatile Carboxymethyl Derivative of Chitosan in Rats: In Vivo and In Vitro Evaluation[J]. Biomacromolecules, 2010, 11(6): 1 527-1 533.

[20]

Zheng M, Han B, Yang Y, et al. Synthesis, Characterization and Biological Safety of O-carboxymethyl Chitosan Used to Treat Sarcoma 180 Tumor[J]. Carbohydrate Polymers, 2011, 86(1): 231-238.

[21]

Lee J, Yun KS, Chang SC, et al. T Cell-Specifc siRNA Delivery Using Antibody-Conjugated Chitosan Nanoparticles[J]. Bioconjug Chem, 2012, 23(6): 1 174-1 180.

[22]

Clogston JD, Patri AK. Zeta Potential Measurement[J]. Methods Mol Biol, 2011, 697(697): 63-70.

[23]

Raveendran R, Bhuvaneshwar GS, Sharma CP. Hemocompatible Curcumin-dextran Micelles as pH Sensitive Pro-drugs for Enhanced Therapeutic Efficacy in Cancer Cells[J]. Carbohydrate Polymers, 2016, 137(1): 597-507.

[24]

Luo Z, Jiang J. pH-sensitive drug Loading/Releasing in Amphiphilic Copolymer PAE-PEG: Integrating Molecular Dynamics and Dissipative Particle Dynamics Simulations[J]. Journal of Controlled Release, 2012, 162(1): 185-193.

[25]

Qiu L, Li Z, Qiao M, et al. Self-assembled pH-responsive Hyaluronic Acid-g-poly((L)-histidine) Copolymer Micelles for Targeted Intracellular Delivery of Doxorubicin[J]. Acta Biomaterialia, 2014, 10(5): 2 024-2 035.

[26]

Rosen H, Abribat T. The Rise and Rise of drug Delivery[J]. Nature Reviews Drug Discovery, 2005, 4(5): 381-385.

[27]

Zhao Y, Yang R, Liu D, et al. Starburst Low-molecular Weight Poly-ethylenimine for Efficient Gene Delivery[J]. Journal of Biomedical Materials Research Part A, 2011, 100A(1): 134-140.

[28]

Gao M, Chen C, Fan A, et al. Stimuli-responsive Polymer-curcumin Conjugate Micelles: Residual Cytotoxicity Analysis[J]. Nanomedicine Nanotechnology Biology & Medicine, 2016, 12(2): 468-468.

[29]

Nordberg J. EGFR Targeting drugs in the Treatment of Head and Neck Squamous Cell Carcinoma[J]. Expert Opinion on Emerging Drugs, 2010, 15(2): 185-201.

[30]

Zhang H, Yun S, Batuwangala TD, et al. A Dual-targeting Antibody Against EGFR-VEGF for Lung and Head and Neck Cancer Treatment[J]. International Journal of Cancer, 2012, 131(4): 956-96.

[31]

Zhou H, Xu H, Li X, et al. Dual Targeting Hyaluronic Acid - RGD Mesoporous Silica Coated Gold Nanorods for Chemo-photothermal Cancer Therapy[J]. Materials Science & Engineering C Materials for Biological Applications, 2017, 81(1): 261-270.

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