Nano-engineered microcapsules boost the treatment of persistent pain

被引:21
|
作者
Kopach, Olga [1 ]
Zheng, Kayiu [1 ]
Dong, Luo [2 ]
Sapelkin, Andrei [3 ]
Voitenko, Nana [4 ]
Sukhorukov, Gleb B. [2 ]
Rusakov, Dmitri A. [1 ]
机构
[1] UCL, UCL Inst Neurol, Dept Clin & Expt Epilepsy, London, England
[2] Queen Mary Univ London, Sch Engn & Mat Sci, London, England
[3] Queen Mary Univ London, Ctr Condensed Matter & Mat Phys, London, England
[4] Bogomoletz Inst Physiol, Dept Sensory Signaling, Kiev, Ukraine
基金
俄罗斯科学基金会; 欧洲研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Biodegradable microcapsules; persistent pain; Na+ channels; drug diffusion; neuronal excitability; pain relief; locomotive deficit and anxiety; DORSAL-HORN NEURONS; REMOTE-CONTROL; DRUG-DELIVERY; CAPSULES; QX-314; NANOPARTICLES; NOCICEPTORS; INHIBITION; RELEASE; SYSTEMS;
D O I
10.1080/10717544.2018.1431981
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Persistent pain remains a major health issue: common treatments relying on either repeated local injections or systemic drug administration are prone to concomitant side-effects. It is thought that an alternative could be a multifunctional cargo system to deliver medicine to the target site and release it over a prolonged time window. We nano-engineered microcapsules equipped with adjustable cargo release properties and encapsulated the sodium-channel blocker QX-314 using the layer-by-layer (LbL) technology. First, we employed single-cell electrophysiology to establish in vitro that microcapsule application can dampen neuronal excitability in a controlled fashion. Secondly, we used two-photon excitation imaging to monitor and adjust long-lasting release of encapsulated cargo in target tissue in situ. Finally, we explored an established peripheral inflammation model in rodents to find that a single local injection of QX-314-containing microcapsules could provide robust pain relief lasting for over a week. This was accompanied by a recovery of the locomotive deficit and the amelioration of anxiety in animals with persistent inflammation. Posthoc immunohistology confirmed biodegradation of microcapsules over a period of several weeks. The overall remedial effect lasted 10-20 times longer than that of a single focal drug injection. It depended on the QX-314 encapsulation levels, involved TRPV1-channel-dependent cell permeability of QX-314, and showed no detectable side-effects. Our data suggest that nano-engineered encapsulation provides local drug delivery suitable for prolonged pain relief, which could be highly advantageous compared to existing treatments.
引用
收藏
页码:435 / 447
页数:13
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