Thakare Mohan, Israel Bridg'ette, Garner Solomon, Ahmed Hisham, Elder Deborah, Capomacchia Anthony
a Department of Pharmaceutical and Biomedical Sciences , University of Georgia , Athens , GA , USA.
b Department of Pharmaceutical Sciences , FAMU , Tallahassee , FL , USA.
Pharm Dev Technol. 2017 May;22(3):418-425. doi: 10.1080/10837450.2016.1221431. Epub 2016 Aug 30.
Evaluate the effects of nonionic surfactants Brij 58 and Tween 40 with different structures but similar hydrophilic lipophilic balances (HLBs) on theophylline (TH)-loaded ethylcellulose (EC) microspheres. Microspheres were formulated using ratios of the surfactants with matching HLB values but different chemical-structures at temperatures (22/35 °C) by hydrophobic solvent-emulsion evaporation. Particle size, GMD, drug loading, encapsulation efficiency and dissolution were evaluated. Drug release was determined using the zero- and first-order, Higuchi and Hixson-Crowell models. EC microspheres prepared with surfactant Brij 58 showed discrete, free-flowing spherical particles, solid interiors and increased particle smoothness as temperature increased; those prepared with Tween 40 appeared porous with coarser surface morphology as temperature increased; both were CHLB (Combined HLB) dependent. Dissolution obeyed the Higuchi model drug release for both microspheres prepared with Tween 40 and Brij 58 except for those prepared with Brij 58 at 35 °C, which presented as zero order. The results were ascribed to the different chemical structure of Brij 58 versus Tween 40 and preparation temperature. Surfactant chemical structure is an unreported processing parameter shown here to be important in microsphere formulation. Brij 58 possesses properties unique to its chemical structure that influence pharmaceutical and molecular biopharmaceutical research.
评估具有不同结构但亲水亲油平衡(HLB)值相似的非离子表面活性剂Brij 58和吐温40对载有茶碱(TH)的乙基纤维素(EC)微球的影响。通过疏水溶剂乳液蒸发法,在(22/35 °C)温度下,使用具有匹配HLB值但化学结构不同的表面活性剂比例来制备微球。评估了粒径、几何平均直径(GMD)、载药量、包封率和溶出度。使用零级和一级、Higuchi和Hixson-Crowell模型测定药物释放。用表面活性剂Brij 58制备的EC微球显示出离散的、自由流动的球形颗粒、实心内部结构,并且随着温度升高颗粒光滑度增加;用吐温40制备的微球随着温度升高表面形态更粗糙且呈现多孔性;两者均依赖于组合HLB(CHLB)。除了在35 °C下用Brij 58制备的微球呈现零级释放外,用吐温40和Brij 58制备的两种微球的溶出均符合Higuchi模型药物释放。结果归因于Brij 58与吐温40的化学结构不同以及制备温度不同。表面活性剂化学结构是一个在此处显示对微球制剂很重要的未报道的加工参数。Brij 58具有其化学结构所特有的性质,这些性质会影响药物和分子生物制药研究。