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一种用于两性霉素B递送的新型聚乙二醇胆烷纳米制剂。

A novel performing PEG-cholane nanoformulation for Amphotericin B delivery.

作者信息

Luengo-Alonso Claudia, Torrado Juan José, Ballesteros Maria Paloma, Malfanti Alessio, Bersani Sara, Salmaso Stefano, Caliceti Paolo

机构信息

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Via F. Marzolo 5, 35131, Italy; Department of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University Complutense of Madrid, Plaza Ramon y Cajal S/N, 28040 Madrid, Spain.

Department of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University Complutense of Madrid, Plaza Ramon y Cajal S/N, 28040 Madrid, Spain.

出版信息

Int J Pharm. 2015 Nov 10;495(1):41-51. doi: 10.1016/j.ijpharm.2015.08.070. Epub 2015 Aug 28.

Abstract

A novel formulation for amphotericin B (AmB) delivery has been developed using micelle-forming 5 kDa monomethoxy-polyethylene glycol functionalized with cholanic acid (PEG 5kDa-cholane). This polymer was found to increase 10(3) times the AmB solubility with a 12:1 AmB/PEG5 kDa-cholane molar ratio (2:1 w/w ratio). Dynamic light scattering and transmission electron microscopy analyses showed that PEG5 kDa-cholane associated with AmB to form 30 nm micelles. Isothermal titration calorimetry analyses performed at different pH showed that PEG 5kDa-cholane interacts with AmB according to multiple-site association profiles. Affinity constants and enthalpy and entropy changes were found to depend on pH, suggesting that the polymer interaction depends on the AmB ionization and aggregation. The freeze-dried product could be promptly re-dispersed forming a colloidal dispersion with the biopharmaceutical features of the freshly prepared micelles, namely AmB solubility and micelle size. The dispersion was stable over one month incubation at room temperature. FT-infrared spectrometry, differential scanning calorimetry and X-ray diffractometry showed that in the freeze-dried product, AmB intimately interacts with PEG 5kDa-cholane. In presence of serum albumin, AmB formulated with PEG 5kDa-cholane was found to undergo less extensive and slower disaggregation than in Fungizone(®). Antifungal activity studies performed using Candida albicans showed that AmB/PEG 5kDa-cholane was 15% more active than AmB in buffer.

摘要

已开发出一种用于两性霉素B(AmB)递送的新型制剂,该制剂使用了用胆酸功能化的形成胶束的5 kDa单甲氧基聚乙二醇(PEG 5kDa-胆烷)。发现该聚合物在AmB与PEG 5kDa-胆烷的摩尔比为12:1(重量比为2:1)时可使AmB的溶解度提高10³倍。动态光散射和透射电子显微镜分析表明,PEG 5kDa-胆烷与AmB结合形成30 nm的胶束。在不同pH下进行的等温滴定量热法分析表明,PEG 5kDa-胆烷根据多位点结合曲线与AmB相互作用。发现亲和常数以及焓和熵的变化取决于pH,这表明聚合物相互作用取决于AmB的电离和聚集。冻干产品可迅速重新分散,形成具有新鲜制备胶束的生物药剂学特征(即AmB溶解度和胶束大小)的胶体分散体。该分散体在室温下孵育一个月仍保持稳定。傅里叶变换红外光谱、差示扫描量热法和X射线衍射法表明,在冻干产品中,AmB与PEG 5kDa-胆烷紧密相互作用。在血清白蛋白存在的情况下,发现用PEG 5kDa-胆烷配制的AmB比在两性霉素B注射剂(Fungizone®)中发生的解聚程度更小且更慢。使用白色念珠菌进行的抗真菌活性研究表明,AmB/PEG 5kDa-胆烷在缓冲液中的活性比AmB高15%。

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