Co-Amorphization, Dissolution, and Stability of Quench-Cooled Drug-Drug Coamorphous Supersaturating Delivery Systems with RT-Unstable Amorphous Components

被引:2
作者
Zhang, Yan-Fei [1 ]
Yao, Qian [2 ]
Lin, Xiao-Ying [1 ]
Ma, Ying-Hui [1 ]
Zhang, Hui-Feng [1 ]
Yu, Huan [1 ]
Mu, Shang-Qiang [3 ]
Zhang, Chuang [1 ]
Geng, Hao [1 ]
Hao, Cheng-Yi [1 ]
Zuo, Li-Li [1 ]
Wu, Di [1 ]
Li, Yue [2 ]
Jin, Li-Li [2 ]
Shi, Nian-Qiu [1 ,2 ]
机构
[1] Jilin Med Univ, Sch Pharm, Jilin 132013, Peoples R China
[2] Yanbian Univ, Coll Pharmaceut Sci, Yanji 133002, Peoples R China
[3] Jilin Med Univ, Affilittend Hosp, Jilin 132011, Peoples R China
关键词
supersaturating drug delivery systems (SDDS); drug-drug" coamorphous system (ddCAM); quench cooling; coamorphization and stability; combination therapy; PHYSICAL STABILITY; ENHANCED DISSOLUTION; SOLUBILITY; BIOAVAILABILITY; INDOMETHACIN;
D O I
10.3390/pharmaceutics16121488
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Supersaturating drug delivery systems (SDDSs) have gained significant attention as a promising strategy to enhance the solubility and bioabsorption of Biopharmaceutics Classification System (BCS) II drugs. To overcome challenges associated with polymer-based amorphous SDDS (aSDDS), coamorphous (CAM) systems have emerged as a viable alternative. Among them, "drug-drug" CAM (ddCAM) systems show considerable potential for combination drug therapy. However, many drugs in their pure amorphous forms are unstable at room temperature (RT), complicating their formation and long-term stability profiles. Consequently, limited knowledge exists regarding the behavior of ddCAMs containing RT-unstable components formed via quench cooling. Methods: In this study, we used naproxen (NAP), a RT-unstable amorphous drug, in combination with felodipine (FEL) or nitrendipine (NTP), two RT-stable amorphous drugs, to create "FEL-NAP" and "NTP-NAP" ddCAM pairs via quench cooling. Our work used a series of methods to perform a detailed analysis on the co-amorphization, dissolution, solubility, and stability profiles of ddCAMs containing RT-unstable drugs, contributing to advancements in co-amorphization techniques for generating SDDS. Results: This study revealed that the co-amorphization and stability profiles of ddCAMs containing RT-unstable components produced via a quench-cooling method were closely related to drug-drug pairing types and ratios. Both quench-cooling and incorporation into coamorphous systems improved the dissolution, solubility, and physical stability of individual APIs. Conclusions: Our findings provide deeper insight into the co-amorphization, dissolution, and stability characteristics of specific drug-drug coamorphous systems FEL-NAP and NTP-NAP, offering valuable guidance for developing new ddCAM coamorphous formulations containing some RT-unstable drugs.
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页数:23
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