Microscopic and spectroscopic evaluation of novel PLGA-chitosan Nanoplexes as an ocular delivery system

被引:50
作者
Jain, Gaurav K. [1 ]
Pathan, Shadab A. [1 ]
Akhter, Sohail [1 ]
Jayabalan, Nirmal [2 ]
Talegaonkar, Sushma [1 ]
Khar, Roop K. [1 ]
Ahmad, Farhan J. [1 ]
机构
[1] Hamdard Univ, Dept Pharmaceut, FO Pharm, New Delhi 110062, India
[2] All India Inst Med Sci, Dept Ocular Pharmacol & Pharm, Dr Rajender Prasad Ctr Ophthalm Sci, New Delhi 110029, India
关键词
Confocal microscopy; Chitosan; Nanoplexes; Ocular drug delivery; PLGA; LOADED BIODEGRADABLE NANOPARTICLES; DRUG-DELIVERY; EPITHELIAL-CELLS; RABBIT; PHARMACOKINETICS; INDOMETHACIN; NANOCARRIERS; NANOCAPSULES; DISPOSITION; NANOSPHERES;
D O I
10.1016/j.colsurfb.2010.09.010
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The interaction of PLGA-chitosan Nanoplexes with ocular mucosa was investigated ex vivo and in vivo to assess their potential as ocular delivery system. Fluorescent Rhodamine Nanoplexes (Rd-Nanoplexes) were prepared by ionotropic gelation method. The size and morphology of Nanoplexes was investigated by TEM, SEM and PCS. The corneal retention, uptake and penetration of Nanoplexes were analyzed by spectrofluorimetry and confocal microscopy. Corneas from Rd-Nanoplexes-treated rabbits were evaluated for the in vivo uptake and ocular tolerance. The Nanoplexes prepared were round with a mean diameter of 115.6 +/- 17 nm and the encapsulation efficiency of Rd was 59.4 +/- 2.5%. Data from ex vivo and in vivo studies showed that the amounts of Rd in the cornea were significantly higher for Nanoplexes than for a control Rd solution, these amounts being fairly constant for up to 24h. Confocal microscopy of the corneas revealed paracellular and transcellular uptake of the Nanoplexes. The uptake mechanism postulated was adsorptive-mediated endocytosis and opening of the tight junctions between epithelial cells. No alteration was microscopically observed after ocular surface exposure to Nanoplexes. Taken together, these data demonstrate that Nanoplexes are potentially useful as ocular drug carriers. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:397 / 403
页数:7
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