肝不全治療のための高効率ビリルビン除去を目的としたイミダゾール官能化四級アンモニウム塩修飾ポリエーテルスルホンミクロスフェア
Ningyue Deng1, Lunqiang Jin2,3, Jing Peng1
1Department of Nephrology, Kidney Research Institute, West China Hospital of Sichuan University, Chengdu, China.
Abstract:
Liver failure can lead to the accumulation of excess bilirubin in the bloodstream, thereby exacerbating disease progression. During the treatment of liver failure, the rapid and efficient adsorption and removal of bilirubin from whole blood via hemoperfusion remain a significant clinical challenge, since whole blood contains not only bilirubin but also other essential components, such as erythrocytes, leukocytes, and platelets. Herein, modified polyethersulfone (PES) microspheres based on the imidazole-functionalized quaternary ammonium salts (IQASs) are fabricated using phase inversion and electrostatic spraying techniques. Subsequently, the adsorption mechanism of the IQASs is systematically investigated, and the modified PES microspheres containing different IQASs are prepared for verification. The prepared hemoperfusion adsorbent (PES/VI8-AANa) achieves a bilirubin clearance ratio exceeding 95% in PBS. Additionally, it achieves a clearance ratio of over 60% within 120 min in plasma, and demonstrates excellent biocompatibility. Furthermore, in animal model validation, the fabricated microspheres exhibit a bilirubin clearance ratio exceeding 50% in whole blood within 120 min, with no significant reduction in albumin and globulin levels. This study presents a systematic and comprehensive methodology aimed at developing a highly efficient whole-blood adsorbent for bilirubin removal, thereby advancing its potential application in clinical therapeutics.
関連する概念動画
Extracorporeal Removal of Drugs: Hemoperfusion and Hemofiltration
Hepatic Drug Excretion: Influencing Factors
Enhanced Elimination of Poison
Antidotes serve a crucial role in counteracting the effects of poison by inhibiting enzymes responsible for producing harmful drug metabolites. In some cases, these toxic metabolites can be neutralized by endogenous cosubstrates, which are maintained at specific concentrations to prevent interaction with cellular macromolecules and subsequent cell death.
Renal excretion is the...
Ion Exchange


