Effect of Hypromellose Acetate Succinate Substituents on Miscibility Behavior of Spray-dried Amorphous Solid Dispersions: Flory-Huggins Parameter Prediction and Validation

被引:15
作者
Jha, Durgesh K. [1 ]
Shah, Devanshi S. [1 ]
Amin, Purnima D. [1 ]
机构
[1] Inst Chem Technol, Dept Pharmaceut Sci & Technol, Matunga 400019, India
来源
CARBOHYDRATE POLYMER TECHNOLOGIES AND APPLICATIONS | 2021年 / 2卷
关键词
HPMCAS substituents; Amorphous solid dispersion; Solubility; Miscibility; Solubility parameter; Flory-Huggins interaction parameter; DRUG-POLYMER MISCIBILITY; HOT-MELT EXTRUSION; DISSOLUTION ENHANCEMENT; SOLUBILITY PARAMETERS; PHYSICAL STABILITY; FORMULATION; HPMCAS; RECRYSTALLIZATION; CONSTRUCTION; TEMPERATURE;
D O I
10.1016/j.carpta.2021.100137
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This study reports the impact of physicochemical properties of lipophilic drugs such as Fenofibrate (FBT), Itraconazole (ITZ), Efavirenz (EFV) and Hydroxypropyl Methylcellulose Acetate Succinate (HPMCAS) grades on the miscibility, dissolution, and stability of the spray dried Amorphous Solid Dispersions (ASDs). The miscibility between of the drugs and HPMCAS grades was predicted using solubility parameter-derived Flory-Huggins interaction parameter and later phase diagram was constructed to delineate the composition dependent miscibility. By varying the HPMCAS grade drug combinations and loadings, the amorphicity of prepared ASDs was analyzed using Differential Scanning Calorimetry (DSC), X-Ray Diffraction (XRD) and in vitro dissolution experiments were conducted to measure apparent solubility and finally, investigate the interplay between sub-stituent ratio and functionality. Interactions between the drugs and polymeric grades and drug concentration in polymer is crucial in determining the drug precipitation within the ASDs which is further supported by Fourier Transform Infrared Spectroscopy (FTIR). The dissolution efficiency and dissolution rate of the ASDs were dependent on the acetyl-succinoyl ratio in HPMCAS.
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页数:11
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