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- W4309557145 endingPage "50" @default.
- W4309557145 startingPage "42" @default.
- W4309557145 abstract "As a promising strategy, amorphous solid dispersion has been extensively employed in improving the oral bioavailability of insoluble drugs. Despite the numerous advantages, the problems associated with supersaturation stability limit its further application. Recently, the formation and stability of the liquid-liquid phase separation drug aggregate (LLPS-DA) have been found to be vital for supersaturation maintenance. An in-depth review of LLPS-DA was required to further explore the supersaturation maintenance mechanism in vivo. Hence, this study aimed to present a short review to introduce the LLPS-DA, highlight the in vivo advantages for oral administration, and discuss the prospects to help understand the in vivo behavior of LLPS-DA." @default.
- W4309557145 created "2022-11-28" @default.
- W4309557145 creator A5000264291 @default.
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- W4309557145 date "2023-01-01" @default.
- W4309557145 modified "2023-10-11" @default.
- W4309557145 title "Liquid–liquid phase separation drug aggregate: Merit for oral delivery of amorphous solid dispersions" @default.
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