Neem seed oil and gum arabic-based oil-in-water emulsions as potential ocular drug delivery system

被引:10
|
作者
Quereshi, Dilshad [1 ]
Dhal, Somali [1 ]
Das, Debasis [2 ]
Mohanty, Biswaranjan [2 ]
Anis, Arfat [3 ]
Shaikh, Hamid [3 ]
Thi Thanh Hanh Nguyen [4 ,5 ]
Kim, Doman [4 ,5 ]
Sarkar, Preetam [6 ]
Pal, Kunal [1 ]
机构
[1] Natl Inst Technol, Dept Biotechnol & Med Engn, Rourkela, India
[2] Inst Pharm & Technol, Salipur, India
[3] King Saud Univ, Dept Chem Engn, Riyadh, Saudi Arabia
[4] Seoul Natl Univ, Dept Int Agr Technol, Seoul, South Korea
[5] Seoul Natl Univ, Inst Green Biosci & Technol, Seoul, South Korea
[6] Natl Inst Technol, Dept Food Proc Engn, Rourkela, India
关键词
Neem seed oil; gum arabic; emulsion; ocular drug delivery; anti-microbial; ciprofloxacin; RELEASE PROPERTIES; EDIBLE FILMS; NANOPARTICLES; GELATIN; HYDROGELS; CHITOSAN; ENCAPSULATION; OPTIMIZATION; FORMULATION; STABILITY;
D O I
10.1080/01932691.2019.1638272
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The present study deciphers the synthesis and characterization of the neem seed oil (NSO) and gum arabic (GA) based emulsion. The synthesized emulsions were thoroughly characterized for probable application in ocular drug delivery. The synthesized emulsions were white in color. The FTIR spectroscopy divulged that the glycoprotein complex of GA retained its functional architecture. The formation of the oil-in-water emulsion was confirmed by confocal microscopy. The NSO droplets in the emulsions behaved as capacitive elements whose properties altered as the composition of the emulsions were varied. The mechanical studies suggested that the interactions within the emulsion components tailored the polymer-polymer integrity under stress. The drug release and corneal permeation studies using ciprofloxacin HCl-loaded emulsions indicated that the ciprofloxacin molecules were released from the emulsions, and the emulsions were able to deliver the drug across the corneal tissue. The prepared emulsions were nonirritant to the ocular tissues. The released drug was capable of inhibiting the growth of the model bacteria (Staphylococcus aureus). In gist, the prepared emulsions were suitable for ocular drug delivery applications. [GRAPHICS] .
引用
收藏
页码:1911 / 1924
页数:14
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