Bimatoprost-loaded lipidic nanoformulation development using quality by design: liposomes versus solid lipid nanoparticles in intraocular pressure reduction

被引:3
|
作者
Verma, Piyush [1 ]
Singh, Rishi Kumar [1 ]
Wadhwa, Anubhav [1 ]
Prabhakar, Bala [1 ]
Yadav, Khushwant S. [1 ]
机构
[1] SVKMs NMIMS Deemed Univ, Shobhaben Pratapbhai Patel Sch Pharm & Technol Man, Mumbai 400056, India
关键词
bimatoprost; design of experiments; in situ hydrogel; IOP reduction; liposomes; quality by design; solid lipid nanoparticles; SUSTAINED OCULAR DELIVERY; QBD-BASED OPTIMIZATION; SITU GELLING SYSTEMS; IN-VITRO; FORMULATION DEVELOPMENT; FACTORIAL DESIGN; RELEASE; GEL;
D O I
10.2217/nnm-2023-0141
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Bimatoprost is a drug used to lower intraocular pressure in the treatment of glaucoma. Conventional eye drops have the limitations of repeated dosing, drug loss due to tear outflow and hence poor availability for action. Materials & methods: Using a systematic quality by design approach, liposomes and solid lipid nanoparticles were formulated and further encapsulated in thermo-sensitive in situ hydrogel. Results & conclusion: Optimized liposomes had 87.04% encapsulation efficiency and 306.78 nm mean particle size, while solid lipid nanoparticles had 90.51% and 304.21 nm. Bimatoprost liposomes had controlled zero-order drug kinetics and no initial burst release, making them better than solid lipid nanoparticles. Bimatoprost-loaded liposomes in thermo-sensitive hydrogel decreased intraocular pressure for 18 h.
引用
收藏
页码:1815 / 1837
页数:23
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