Ocular Delivery of Bimatoprost-Loaded Solid Lipid Nanoparticles for Effective Management of Glaucoma

被引:11
|
作者
Satyanarayana, Sandeep Divate [1 ]
Abu Lila, Amr Selim [2 ,3 ]
Moin, Afrasim [3 ]
Moglad, Ehssan H. [4 ,5 ]
Khafagy, El-Sayed [4 ,6 ]
Alotaibi, Hadil Faris [7 ]
Obaidullah, Ahmad J. [8 ]
Charyulu, Rompicherla Narayana [1 ]
机构
[1] Nitte, NGSM Inst Pharmaceut Sci, Dept Pharmaceut, Mangalore 575018, India
[2] Zagazig Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Zagazig 44519, Egypt
[3] Univ Hail, Coll Pharm, Dept Pharmaceut, Hail 81442, Saudi Arabia
[4] Prince Sattam Bin Abdulaziz Univ, Coll Pharm, Dept Pharmaceut, Al Kharj 11942, Saudi Arabia
[5] Natl Ctr Res, Med & Aromat Plants Res Inst, Dept Microbiol & Parasitol, Khartoum 2404, Sudan
[6] Suez Canal Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Ismailia 41522, Egypt
[7] Princess Nourah Bint Abdul Rahman Univ, Coll Pharm, Dept Pharmaceut Sci, Riyadh 11671, Saudi Arabia
[8] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh 11451, Saudi Arabia
关键词
bimatoprost; central composite design; glaucoma; HET-CAM test; solid lipid nanoparticles (SLNs); FORMULATION; OPTIMIZATION; RELEASE; CARRIERS; SYSTEM;
D O I
10.3390/ph16071001
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glaucoma is a progressive optic neuropathy characterized by a rise in the intraocular pressure (IOP) leading to optic nerve damage. Bimatoprost is a prostaglandin analogue used to reduce the elevated IOP in patients with glaucoma. The currently available dosage forms for Bimatoprost suffer from relatively low ocular bioavailability. The objective of this study was to fabricate and optimize solid lipid nanoparticles (SLNs) containing Bimatoprost for ocular administration for the management of glaucoma. Bimatoprost-loaded SLNs were fabricated by solvent evaporation/ultrasonication technique. Glyceryl Monostearate (GMS) was adopted as solid lipid and poloxamer 407 as surfactant. Optimization of SLNs was conducted by central composite design. The optimized formulation was assessed for average particle size, entrapment efficiency (%), zeta potential, surface morphology, drug release study, sterility test, isotonicity test, Hen's egg test-chorioallantoic membrane (HET-CAM) test and histopathology studies. The optimized Bimatoprost-loaded SLNs formulation had an average size of 183.3 & PLUSMN; 13.3 nm, zeta potential of -9.96 & PLUSMN; 1.2 mV, and encapsulation efficiency percentage of 71.8 & PLUSMN; 1.1%. Transmission electron microscopy (TEM) study revealed the nearly smooth surface of formulated particles with a nano-scale size range. In addition, SLNs significantly sustained Bimatoprost release for up to 12 h, compared to free drug (p < 005). Most importantly, HET-CAM test nullified the irritancy of the formulation was verified its tolerability upon ocular use, as manifested by a significant reduction in mean irritation score, compared to positive control (1% sodium dodecyl sulfate; p < 0.001). Histopathology study inferred the absence of any signs of cornea tissue damage upon treatment with Bimatoprost optimized formulation. Collectively, it was concluded that SLNs might represent a viable vehicle for enhancing the corneal permeation and ocular bioavailability of Bimatoprost for the management of glaucoma.
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页数:15
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