用于抗体持续释放的负载抗体的阳离子多孔PLGA微粒的制备和表征。

IF 5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Ayaka Hanaki, Koki Ogawa, Tatsuaki Tagami, Tetsuya Ozeki
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引用次数: 0

摘要

聚乳酸-乙醇酸(PLGA)微粒已被配制成允许包括抗体在内的多种药物的持续释放。众所周知,抗体易受化学和物理压力的影响;因此,有必要在温和的条件下负载在PLGA微粒上。在本研究中,我们构建了阳离子多孔PLGA微粒,该微粒可以用英夫利昔单抗作为模型抗体静电吸附。以聚乙烯亚胺和碳酸氢铵为原料,采用双乳液法制备了阳离子多孔PLGA微粒。抗体负载后,通过温和加热实现表面孔隙闭合。优化配方的尺寸约为5μm,显示出正电荷。负载的抗体在56天内逐渐从制剂中释放。基于肿瘤坏死因子(TNF)-α抑制测定,释放的英夫利昔单抗保持其药理学活性。总之,我们成功地将抗体装载到PLGA微粒中,同时保持活性并展示出长效特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fabrication and Characterization of Antibody-Loaded Cationic Porous PLGA Microparticles for Sustained Antibody Release.

Fabrication and Characterization of Antibody-Loaded Cationic Porous PLGA Microparticles for Sustained Antibody Release.

Poly lactic-co-glycolic acid (PLGA) microparticles have been formulated to allow the sustained release of numerous drugs, including antibodies. It is well-known that antibodies are susceptible to chemical and physical stress; therefore, it is necessary to be loaded on PLGA microparticles under mild conditions. In the present study, we constructed cationic porous PLGA microparticles that could be electrostatically adsorbed with infliximab as a model antibody. Cationic porous PLGA microparticles were prepared using the double emulsion method by adding polyethyleneimine and ammonium bicarbonate. After antibody loading, surface pores closure was achieved by mild heating. The size of the optimized formulation was approximately 5 μm, exhibiting a positive charge. The loaded antibody was gradually released from the formulation over 56 days. Based on a tumor necrosis factor (TNF)-α inhibition assay, the released infliximab maintained its pharmacological activity. Collectively, we successfully loaded antibodies into PLGA microparticles while maintaining activity and demonstrating long-acting properties.

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来源期刊
AAPS Journal
AAPS Journal 医学-药学
CiteScore
7.80
自引率
4.40%
发文量
109
审稿时长
1 months
期刊介绍: The AAPS Journal, an official journal of the American Association of Pharmaceutical Scientists (AAPS), publishes novel and significant findings in the various areas of pharmaceutical sciences impacting human and veterinary therapeutics, including: · Drug Design and Discovery · Pharmaceutical Biotechnology · Biopharmaceutics, Formulation, and Drug Delivery · Metabolism and Transport · Pharmacokinetics, Pharmacodynamics, and Pharmacometrics · Translational Research · Clinical Evaluations and Therapeutic Outcomes · Regulatory Science We invite submissions under the following article types: · Original Research Articles · Reviews and Mini-reviews · White Papers, Commentaries, and Editorials · Meeting Reports · Brief/Technical Reports and Rapid Communications · Regulatory Notes · Tutorials · Protocols in the Pharmaceutical Sciences In addition, The AAPS Journal publishes themes, organized by guest editors, which are focused on particular areas of current interest to our field.
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