Patel Sulabh P, Vaishya Ravi, Patel Ashaben, Agrahari Vibhuti, Pal Dhananjay, Mitra Ashim K
a Division of Pharmaceutical Sciences, School of Pharmacy , University of Missouri-Kansas City , Kansas City , MO , USA.
J Microencapsul. 2016;33(2):103-13. doi: 10.3109/02652048.2015.1134685. Epub 2016 Mar 11.
This manuscript is focussed on the development of pentablock (PB) copolymer based sustained release formulation for the treatment of posterior segment ocular diseases. We have successfully synthesised biodegradable and biocompatible PB copolymers for the preparation of nanoparticles (NPs) and thermosensitive gel. Achieving high drug loading with hydrophilic biotherapeutics (peptides/proteins) is a challenging task. Moreover, small intravitreal injection volume (≤100 μL) requires high loading to develop a long term (six months) sustained release formulation. We have successfully investigated various formulation parameters to achieve maximum peptide/protein (octreotide, insulin, lysozyme, IgG-Fab, IgG, and catalase) loading in PB NPs. Improvement in drug loading can facilitate delivery of larger doses of therapeutic proteins via limited injection volume. A composite formulation comprised of NPs in gel system exhibited sustained release (without burst effect) of peptides and proteins, may serve as a platform technology for the treatment of posterior segment ocular diseases.
本手稿聚焦于开发基于五嵌段(PB)共聚物的缓释制剂,用于治疗眼后段疾病。我们已成功合成了可生物降解且生物相容的PB共聚物,用于制备纳米颗粒(NPs)和热敏凝胶。实现亲水性生物治疗剂(肽/蛋白质)的高载药量是一项具有挑战性的任务。此外,玻璃体内注射体积小(≤100 μL)需要高载药量来开发长期(六个月)缓释制剂。我们已成功研究了各种制剂参数,以在PB NPs中实现最大肽/蛋白质(奥曲肽、胰岛素、溶菌酶、IgG-Fab、IgG和过氧化氢酶)载药量。载药量的提高可通过有限的注射体积促进更大剂量治疗性蛋白质的递送。由凝胶系统中的NPs组成的复合制剂表现出肽和蛋白质的缓释(无突释效应),可作为治疗眼后段疾病的平台技术。