Amorphous solid dispersion to facilitate the delivery of poorly water-soluble drugs: recent advances on novel preparation processes and technology coupling

被引:0
作者
Luo, Chengxiang [1 ]
Li, Ruipeng [2 ]
Tang, Mi [2 ,3 ]
Gao, Yuan [2 ]
Zhang, Jianjun [1 ]
Qian, Shuai [2 ]
Wei, Yuanfeng [2 ]
Shen, Peiya [2 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, Nanjing, Peoples R China
[2] China Pharmaceut Univ, Sch Tradit Chinese Pharm, 639 Longmian Ave, Nanjing 211198, Peoples R China
[3] Jiangsu Litaier Pharm Ltd, Nanjing, Peoples R China
基金
中国国家自然科学基金;
关键词
Amorphous solid dispersion; technology coupling; preparation process; permeability; solubility; mechanism; bioavailability; HOT-MELT EXTRUSION; PRESSURIZED CARBON-DIOXIDE; SPRAY-DRYING FORMULATION; PH-DEPENDENT SOLUBILITY; ENHANCED BIOAVAILABILITY; MICROENVIRONMENTAL PH; DISSOLUTION BEHAVIOR; MOLECULAR MOBILITY; PHYSICAL STABILITY; ORAL ABSORPTION;
D O I
10.1080/17425247.2024.2423813
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionAmorphous solid dispersion (ASD) technique has recently been used as an effective formulation strategy to significantly improve the bioavailability of insoluble drugs. The main industrialized preparation methods for ASDs are mainly hot melt extrusion and spray drying techniques; however, they face the limitations of being unsuitable for heat-sensitive materials and organic reagent residues, respectively, and therefore novel preparation processes and technology coupling for developing ASDs have received increasing attention.Areas coveredThis paper reviews recent advances in ASD and provides an overview of novel preparation methods, mechanisms for improving drug bioavailability, and especially technology coupling.Expert coveredAs a mature pharmaceutical technology, ASD has broad application prospects and values. During the period from 2012 to 2024, the FDA has approved 49 formulation products containing ASDs. However, with the diversification of drug types and clinical needs, the traditional formulation technology of ASDs is gradually no longer sufficient to meet the needs of clinical medication. Therefore, this review summarizes the studies on both novel preparation processes and technology combinations; and provides a comprehensive overview of the mechanisms of ASD to improve drug bioavailability, in order to better select appropriate preparation methods for the development of ASD formulations.
引用
收藏
页码:1807 / 1822
页数:16
相关论文
共 149 条
[1]   Personalization of lipid-based oral dosage forms via filament-based 3D-printing [J].
Abdelhamid, Moaaz ;
Corzo, Carolina ;
Urich, Jesus Alberto Afonso ;
Slama, Eyke ;
Froehlich, Eleonore ;
Lochmann, Dirk ;
Reyer, Sebastian ;
Freichel, Tanja ;
Spoerk, Martin ;
Salar-Behzadi, Sharareh .
APPLIED MATERIALS TODAY, 2024, 40
[2]   Electrospun nanofibers: Exploring process parameters, polymer selection, and recent applications in pharmaceuticals and drug delivery [J].
Abdulhussain, Rand ;
Adebisi, Adeola ;
Conway, Barbara R. ;
Asare-Addo, Kofi .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2023, 90
[3]   Advances in Light-Responsive Smart Multifunctional Nanofibers: Implications for Targeted Drug Delivery and Cancer Therapy [J].
Agiba, Ahmed M. ;
Elsayyad, Nihal ;
ElShagea, Hala N. ;
Metwalli, Mahmoud A. ;
Mahmoudsalehi, Amin Orash ;
Beigi-Boroujeni, Saeed ;
Lozano, Omar ;
Aguirre-Soto, Alan ;
Arreola-Ramirez, Jose Luis ;
Segura-Medina, Patricia ;
Hamed, Raghda Rabe .
PHARMACEUTICS, 2024, 16 (08)
[4]   Melt Fusion Techniques for Solubility Enhancement: A Comparison of Hot Melt Extrusion and KinetiSol® Technologies [J].
Ajjarapu, Srinivas ;
Banda, Srikanth ;
Basim, Pratap ;
Dudhipala, Narendar .
SCIENTIA PHARMACEUTICA, 2022, 90 (03)
[5]   A Rundown Through Various Methods Used in the Formulation of Solid Self-Emulsifying Drug Delivery Systems (S-SEDDS) [J].
Almeida, Sharel Rency D. ;
Tippavajhala, Vamshi Krishna .
AAPS PHARMSCITECH, 2019, 20 (08)
[6]   Hot-Melt extrusion coupled with pressurized carbon dioxide for enhanced processability of pharmaceutical polymers and drug delivery applications-An integrated review [J].
Almutairi, Mashan ;
Srinivasan, Priyanka ;
Zhang, Peilun ;
Austin, Fischer ;
Butreddy, Arun ;
Alharbi, Muteb ;
Bandari, Suresh ;
Ashour, Eman A. ;
Repka, Michael A. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2022, 629
[7]   An investigation into the formations of the internal microstructures of solid dispersions prepared by hot melt extrusion [J].
Alqahtani, Fahad ;
Belton, Peter ;
Bin Zhang ;
Al-Sharabi, Mohammed ;
Ross, Steven ;
Mithu, Md Sadeque Hossain ;
Douroumis, Dionysios ;
Zeitler, J. Axel ;
Qi, Sheng .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2020, 155 :147-161
[8]   Melt Extrusion of High-Dose Co-Amorphous Drug-Drug Combinations [J].
Arnfast, Laerke ;
Kamruzzaman, Md ;
Lobmann, Korbinian ;
Aho, Johanna ;
Baldursdottir, Stefania ;
Rades, Thomas ;
Rantanen, Jukka .
PHARMACEUTICAL RESEARCH, 2017, 34 (12) :2689-2697
[9]   Influence of pressurized carbon dioxide on ketoprofen-incorporated hot-melt extruded low molecular weight hydroxypropylcellulose [J].
Ashour, Eman A. ;
Kulkarni, Vijay ;
Almutairy, Bjad ;
Park, Jun-Bom ;
Shah, Sejal P. ;
Majumdar, Soumyajit ;
Lian, Zhuoyang ;
Pinto, Elanor ;
Bi, Vivian ;
Durig, Thomas ;
Martin, Scott T. ;
Repka, Michael A. .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2016, 42 (01) :123-130
[10]   Microenvironmental pH modulation in solid dosage forms [J].
Badawy, Sherif I. Farag ;
Hussain, Munir A. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (05) :948-959