Preparation of PLLA/bpV(pic) microspheres and their effect on nerve cells

Qiang Lin , Hai-yun Chen , Hao-shen Li , Yang-ting Cai

Current Medical Science ›› 2014, Vol. 34 ›› Issue (1) : 76 -80.

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Current Medical Science ›› 2014, Vol. 34 ›› Issue (1) : 76 -80. DOI: 10.1007/s11596-014-1234-z
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Preparation of PLLA/bpV(pic) microspheres and their effect on nerve cells

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Abstract

In this study, we prepared PLLA/bpV(pic) microspheres, a bpV(pic) controlled release system and examined their ability to protect nerve cells and promote axonal growth. PLLA microspheres were prepared by employing the o/w single emulsification-evaporation technique. Neural stem cells and dorsal root ganglia were divided into 3 groups in terms of the treatment they received: a routine medium group (cultured in DMEM), a PLLA microsphere group (DMEM containing PLLA microspheres alone) and a PLLA/bpV(pic) group [DMEM containing PLLA/bpV(pic) microspheres]. The effects of PLLA/bpV(pic) microspheres were evaluated by the live-dead test and measurement of axonal length. Our results showed that PLLA/bpV(pic) granulation rate was (88.2±5.6)%; particle size was (16.8±3.1)%, drug loading was (4.05±0.3)%; encapsulation efficiency was (48.5±1.8)%. The release time lasted for 30 days. In PLLA/bpV(pic) microsphere group, the cell survival rate was (95.2 ±4.77)%, and the length of dorsal root ganglion (DRG) was 718±95 μm, which were all significantly greater than those in ordinary routine medium group and PLLA microsphere group. This preliminary test results showed the PLLA/bpV(pic) microspheres were successfully prepared and they could promote the survival and growth of neural cells in DRG.

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microspheres / PLLA/bpV(pic) / controlled release / neural stem cells / dorsal root ganglion

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Qiang Lin, Hai-yun Chen, Hao-shen Li, Yang-ting Cai. Preparation of PLLA/bpV(pic) microspheres and their effect on nerve cells. Current Medical Science, 2014, 34(1): 76-80 DOI:10.1007/s11596-014-1234-z

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References

[1]

ParkKK, LiuK, HuY, et al.. Promoting axon regeneration in the adult CNS by modulation of the PTEN/mTOR pathway. Science, 2008, 322(5903): 963-966

[2]

ChristieKJ, WebberCA, MartinezJA, et al.. PTEN inhibition to facilitate intrinsic regenerative outgrowth of adult peripheral axons. J Neurosci, 2010, 30(27): 9306-9315

[3]

WalkerCL, WalkerMJ, LiuNK, et al.. Systemic bisperoxovanadium activates Akt/mTOR, reduces autophagy, and enhances recovery following cervical spinal cord injury. PLoS One, 2012, 7(1): e30012

[4]

YangP. Promoting the repair of CNS by targeting PTEN. Prog Phys Sci (Chinese), 2010, 41(4): 313-316s

[5]

AbeN, BorsonSH, GambelloMJ, et al.. Mammalian target of rapamycin (mTOR) activation increases axonal growth capacity of injured peripheral nerves. J Biol Chem, 2010, 285(36): 28 034-28 043

[6]

LiuK, LuY, LeeJK, et al.. PTEN deletion enhances the regenerative ability of adult corticospinal neurons. Nat Neurosci, 2010, 13(9): 1075-1081

[7]

KurimotoT, YinY, OmuraK, et al.. Long-distance axon regeneration in the mature optic nerve: contributions of oncomodulin, cAMP, and pten gene deletion. J Neurosci, 2010, 30(46): 15654-15663

[8]

ZhuY, HoellP, AhlemeyerB, et al.. Implication of PTEN in production of reactive oxygen species and neuronal death in in vitro models of stroke and Parkinson’s disease. Neurochem Int, 2007, 50(3): 507-516

[9]

WuHR, WangYC, CaiQY. Roles of PTEN in neuronal injury and brain disorders. Yixue Zongshu (Chinese), 2010, 16(11): 1607-1610

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