dorzolamide负载6-o-羧甲基壳聚糖纳米颗粒治疗开角型青光眼的研制。

Journal of drug delivery Pub Date : 2013-01-01 Epub Date: 2013-10-10 DOI:10.1155/2013/562727
Ujwala Shinde, Mohammed Hadi Ahmed, Kavita Singh
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引用次数: 40

摘要

壳聚糖(CS)是一种生物可降解、生物相容性强、黏附性强的天然聚合物,仅在酸性环境中可溶,对眼睛有刺激性。本研究的目的是合成盐酸多唑胺(dorzolamide hydrochloride, DRZ)的水溶性6- o -羧甲基(OCM-CS)衍生物,并制备载药于盐酸多唑胺(dorzolamide hydrochloride, DRZ)的6- o -羧甲基纳米粒子(NPs)。CS与一氯乙酸(MCA)反应合成OCM-CS,并通过FT-IR、DSC和(13)C NMR进行了表征。采用离子凝胶法制备了CS和OCM-CS NPs。采用降低正常血压家兔眼压的方法评估眼刺激电位,并测定治疗效果。在55℃条件下,水与异丙醇的比例为1/4时收率最高。FT-IR, DSC和(13)C NMR证实了CS和MCA羟基之间形成醚键。优化后的CSNPs粒径为250.3±2.62 nm, zeta电位为+33.47±0.723 mV,而OCM-CSNPs粒径为187.1±2.72 nm, zeta电位为30.87±0.86 mV。与csnp相比,ocm - csnp的捕获效率显著提高。与csnp相比,ocm - csnp具有量身定制的药物释放和提高的生物利用度,减少了脉冲进入。因此,可以得出结论,DRZ加载ocm - csnp将是现有眼药水治疗青光眼的更好选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of dorzolamide loaded 6-o-carboxymethyl chitosan nanoparticles for open angle glaucoma.

Development of dorzolamide loaded 6-o-carboxymethyl chitosan nanoparticles for open angle glaucoma.

Development of dorzolamide loaded 6-o-carboxymethyl chitosan nanoparticles for open angle glaucoma.

Development of dorzolamide loaded 6-o-carboxymethyl chitosan nanoparticles for open angle glaucoma.

Chitosan (CS) is a biodegradable, biocompatible, and mucoadhesive natural polymer soluble in acidic pH only and can be irritating to the eye. Objective of the study was to synthesize water soluble 6-O-carboxymethyl (OCM-CS) derivative of CS, and to develop CS and OCM-CS nanoparticles (NPs) loaded with dorzolamide hydrochloride (DRZ). CS was reacted with monochloroacetic acid (MCA) for OCM-CS synthesis and was characterized by FT-IR, DSC, and (13)C NMR. CS and OCM-CS NPs were prepared by ionic gelation method. Ocular irritation potential were evaluated and therapeutic efficacy was measured by reduction in intraocular pressure (IOP) in normotensive rabbits. Maximum yield was obtained when the ratio of water/isopropyl alcohol was 1/4 at 55°C. The FT-IR, DSC and (13)C NMR confirmed the formation of an ether linkage between hydroxyl groups of CS and MCA. The particle size and zeta potential of optimised CSNPs was 250.3 ± 2.62 nm and +33.47 ± 0.723 mV, whereas those for OCM-CSNPs were 187.1 ± 2.72 nm and 30.87 ± 0.86 mV. The entrapment efficiency was significantly improved for OCM-CSNPs, compared to CSNPs. OCM-CSNPs had tailored drug release and improved bioavailability with reduction in pulse entry as compared to CSNPs. Hence, it can be concluded that DRZ loaded OCM-CSNPs would be better alternative option to available eye drops for glaucoma treatment.

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来源期刊
Journal of drug delivery
Journal of drug delivery PHARMACOLOGY & PHARMACY-
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