Darole Pradnya S, Hegde Darshana D, Nair Hema A
Department of Pharmaceutics, Bombay College of Pharmacy, Kalina, Santacruz (E.), Mumbai 400098, Maharashtra, India.
AAPS PharmSciTech. 2008;9(1):122-8. doi: 10.1208/s12249-007-9022-8. Epub 2008 Jan 18.
The present studies were designed to develop a formulation of amphotericin B in a lipid-based preparation as a microemulsion and to compare its toxicity with the commercial formulation Fungizone. The final product developed is a lyophilized amphotericin B, oil and surfactant blend for reconstitution in water to yield a microemulsion containing 5 mg/ml of the drug. Pseudoternary phase diagrams were constructed to identify areas of existence of microemulsion composed of Peceol (glyceryl monooleate) as oil phase and Mys 40 (polyethylene glycol 40 stearate) and Solutol HS 15 (polyethylene glycol 15 hydroxy stearate) as surfactants. Amphotericin B was co-evaporated with oil - surfactant mixture to produce a microemulsion pre-concentrate. The co-evaporate was diluted in water, filtered for sterilization and lyophilized to obtain the final product. The lyophilized as well as the reconstituted products were separately studied for stability and the latter was also characterized for various physicochemical aspects including droplet size of the dispersed phase, osmolarity and aggregation state of drug. The dispersion showed no evidence of precipitation of drug for 48 h, and resisted destabilization due to freeze-thaw cycles or centrifugation. The dispersed phase globules measured a mean size of 84 nm and uv-spectrophotometric studies indicated the presence of self-aggregated amphotericin B. The present formulation showed a 92% decrease in haemolysis of human RBC in vitro when compared with the commercially available Fungizone. The LD(50) in mice was estimated to be 3.4 mg/kg. The results indicate that the formulation holds promise for development as a safer and efficacious alternative for amphotericin B therapy.
本研究旨在开发一种两性霉素B脂质体制剂微乳,并将其毒性与市售制剂两性霉素B注射剂进行比较。最终产品是冻干的两性霉素B、油和表面活性剂混合物,用于在水中复溶以产生含5mg/ml药物的微乳。构建伪三元相图以确定由油酸甘油酯作为油相、聚乙二醇40硬脂酸酯和聚乙二醇15羟基硬脂酸酯作为表面活性剂组成的微乳的存在区域。两性霉素B与油-表面活性剂混合物共蒸发以制备微乳预浓缩物。将共蒸发物用水稀释,过滤除菌并冻干以获得最终产品。分别研究了冻干产品和复溶产品的稳定性,复溶产品还对包括分散相液滴大小、渗透压和药物聚集状态在内的各种物理化学方面进行了表征。分散液在48小时内未显示药物沉淀迹象,并且抵抗了冻融循环或离心引起的失稳。分散相小球的平均大小为84nm,紫外分光光度法研究表明存在自聚集的两性霉素B。与市售的两性霉素B注射剂相比,本制剂在体外对人红细胞的溶血作用降低了92%。小鼠的半数致死量估计为3.4mg/kg。结果表明,该制剂有望开发成为两性霉素B治疗更安全有效的替代品。