The Role of Glass Transition Temperatures in Coamorphous Drug–Amino Acid Formulations

药品 玻璃化转变 过渡(遗传学) 化学 立体化学 色谱法 有机化学 药理学 生物化学 医学 聚合物 基因
作者
Eric Ofosu Kissi,Georgia Kasten,Korbinian Löbmann,Thomas Rades,Holger Grohganz
出处
期刊:Molecular Pharmaceutics [American Chemical Society]
卷期号:15 (9): 4247-4256 被引量:51
标识
DOI:10.1021/acs.molpharmaceut.8b00650
摘要

The improved physical stability associated with coamorphous drug–amino acid (AA) formulations may indicate a decrease in mobility of the amorphous drug molecules, compared to the neat amorphous form of the drug. Since the characteristic glass transition temperatures (Tgα and Tgβ) represent molecular mobility in amorphous systems, we aimed to characterize Tgα and Tgβ and to determine their role in physical stability as well as their potential usefulness to determine the presence of an excess component (either drug or AA) in coamorphous systems. Indomethacin (IND)–tryptophan (TRP) and carvedilol (CAR)–TRP were used as model coamorphous systems. The analytical techniques used were X-ray powder diffractometry (XRPD) to determine the solid-state form, dynamic mechanical analysis (DMA) to probe Tgα and Tgβ, and differential scanning calorimetry (DSC) to probe thermal behavior of the coamorphous systems. Tgα analysis showed a gradual monotonous increase in Tgα values with increasing AA concentration, and this increase in the Tgα value is not the cause of the improved physical stability. The Tgβ analysis for the IND–TRP sample with 10% drug had a Tgβ of 226.8 K, and samples with 20–90% drug had similar Tgβ values around 212.5 K. For CAR–TRP, samples with 10–40% drug had similar Tgβ values around 230.5 K, and samples with 50–90% drug had similar Tgβ values around 223.3 K. The similar Tgβ values in coamorphous systems at different drug ratios indicate that they in fact are the Tgβ of the component that is in excess to an ideal drug–AA coamorphous mixture. DSC and XRPD analysis showed that for IND–TRP, IND is in excess if the drug concentration is 30% or above and will eventually recrystallize. For CAR–TRP, CAR is in excess and recrystallizes when the drug concentration is 50% or above. We have proposed a means of estimating, on the basis of Tgβ, which drug to AA ratios will lead to optimally physically stable coamorphous systems that can be considered for further development.
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