Effect of pH modifiers on the solubility, dissolution rate, and stability of telmisartan solid dispersions produced by hot-melt extrusion technology

被引:22
|
作者
Almotairy, Ahmed [1 ,2 ]
Almutairi, Mashan [1 ,3 ]
Althobaiti, Abdulmajeed [1 ]
Alyahya, Mohammed [1 ,4 ]
Sarabu, Sandeep [1 ]
Alzahrani, Abdullah [1 ]
Zhang, Feng [5 ]
Bandari, Suresh [1 ]
Repka, Michael A. [1 ,6 ]
机构
[1] Univ Mississippi, Sch Pharm, Dept Pharmaceut & Drug Delivery, University, MS 38677 USA
[2] Taibah Univ, Coll Pharm, Pharmaceut & Pharmaceut Technol Dept, Al Madinah Al Munawarah 30001, Saudi Arabia
[3] Univ Hail, Coll Pharm, Dept Pharmaceut, Hail 81442, Saudi Arabia
[4] King Saud Univ, Coll Pharm, Dept Pharmaceut, Riyadh 11451, Saudi Arabia
[5] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA
[6] Univ Mississippi, Pii Ctr Pharmaceut Technol, University, MS 38677 USA
关键词
Hot-melt extrusion; Design of experiments; Microenvironmental pH; Telmisartan; Solubility enhancement; HPMCASLG; WATER-SOLUBLE DRUG; PHYSICAL STABILITY; ACETATE SUCCINATE; TABLETS; FORMULATION; ALKALIZERS; DELIVERY; BEHAVIOR; RELEASE; CARRIER;
D O I
10.1016/j.jddst.2021.102674
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the current study was to investigate the dual effect of an amorphous solid dispersion generated by hot melt extrusion and the addition of pH modifiers on the solubility and stability of telmisartan. Hydroxypropyl methylcellulose acetate succinate L grade was used as a polymeric carrier and recrystallization inhibitor, and meglumine, sodium carbonate, or Neusilin S2 were incorporated as pH modifiers to generate a desirable microenvironmental pH in the solid dispersions. Differential scanning calorimetry, powder X-ray diffraction, and Fourier transform infrared spectroscopy were incorporated to obtain the solid-state characterizations of telmisartan, and the results confirm a partial transformation of telmisartan to an amorphous state. An in vitro release study revealed that the transformation of telmisartan to an amorphous material improved its dissolution rate by 2-fold compared to pure drug and by up to 5-fold with the incorporation of pH modifiers. Results of the stability studies demonstrated that the samples have no significant degradation under accelerated stability conditions at 40 degrees C/75% RH.
引用
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页数:10
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