Tenoxicam-loaded polymeric micelles material: Formulation, optimization, and evaluation

被引:8
|
作者
Hussein, Hussein A. Abdul [1 ]
Maraie, Nidhal K. [2 ]
机构
[1] Baghdad Coll Med Sci, Dept Pharmaceut, Baghdad, Iraq
[2] Mustansiriyah Univ, Coll Pharm, Dept Pharmaceut, Baghdad, Iraq
关键词
Tenoxicam; Poloxamer; 407; Thin-film hydration method; Entrapment efficacy; Solubility; Polymeric micelles; BLOCK-COPOLYMER MICELLES; DRUG-DELIVERY; IN-VITRO; MIXED MICELLES; ORAL BIOAVAILABILITY; DISSOLUTION; SOLUBILITY; F127; ENHANCEMENT; CURCUMIN;
D O I
10.1016/j.matpr.2021.08.218
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The objective of the current study was to encapsulate Tenoxicam a poorly soluble drug within selfassembled polymeric micelles created from amphiphilic block copolymer poloxamer 407 to enhance its solubility and thus increasing oral bioavailability. Thin-film hydration technique was adapted in preparation of Tenoxicam loaded polymeric micelles based on different ratios of copolymer poloxamer 407 (ranging from 1:5 up to 1:90), selection of the best micellar formula was based on the values of entrapment efficiency (EE%), particle size (PS), polydispersity index (PDI), and rate of in vitro drug release, then lyophilization was done for selected formula. Prepared micellar solutions (PM1-PM10) were characterized and the best formula PM6 was chosen according to good EE% (84.05%), smaller particle size (33. 07 +/- 2.23 nm), lower PDI value (0.155), and higher in vitro drug release (81.43% +/- 0.048), which further lyophilized and subjected for powder characterization. Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) indicated that TNX was encapsulated in polymeric micelle core, due to the disappearance of a characteristic peak of TNX. Saturated solubility of PM6 lyophilized powder showed an increase in aqueous solubility (122 times) compared with pure drug, while transmission electron microscopy (TEM) showed the polymeric micelles in images with a spherical structure, smooth surface, uniform particle size, and homogeneous distribution in an aqueous medium. It was concluded that the prepared amphiphilic copolymer micelles loaded with TNX exhibited significant improvement in drug solubility and consequently may enhance oral bioavailability and suggested to be used to prepare solid oral dosage form as an alternative to the marketed one with lower dose size and reduce drug side effects. Copyright (c) 2022 Elsevier Ltd. All rights reserved. Selection and peer-review under responsibility of the scientific committee of the International Conference on Recent Advances in Mechanical Engineering and Nanomaterials
引用
收藏
页码:672 / 680
页数:9
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