中国医药生物技术
中國醫藥生物技術
중국의약생물기술
CHINESE MEDICINAL BIOTECHNOLOGY
2014年
3期
196-201
,共6页
降钙素%泊洛沙姆%温度敏感原位凝胶
降鈣素%泊洛沙姆%溫度敏感原位凝膠
강개소%박락사모%온도민감원위응효
Calcitonin%Poloxamer%Thermosensitive in situ gel
目的构建鲑鱼降钙素新型注射用温度敏感原位凝胶系统并对其胶凝特性和降血钙效应进行评价。<br> 方法以泊洛沙姆 F127为主要基质材料,复合使用泊洛沙姆 F68,制备鲑鱼降钙素注射用温度敏感原位凝胶给药系统,以胶凝温度、胶凝时间、流变学、质构特性为考察指标,对该凝胶系统性质进行评价;采用大鼠眼眶取血,钙显色法监测体内血清钙离子浓度,对该凝胶系统降血钙效应进行研究。<br> 结果所制备的鲑鱼降钙素注射用温度敏感原位凝胶的胶凝温度为(35.3±1.3)℃,胶凝时间为(108.3±5.5)s,在25℃条件下为流动的液体,原位凝胶的黏度和黏滞力极低,方便注射给药,当温度增至37℃时能够迅速发生相转变,黏度和黏滞力等质构特性数据显著增加,成为具有一定胶凝强度的半固体;大鼠降血钙效应结果显示,该给药系统具有明显的缓释作用,其24 h 时血钙浓度明显低于普通注射剂组,相对于普通注射剂的药理活性为138.6%。<br> 结论温度敏感原位凝胶用于鲑鱼降钙素的注射给药,是一种很有潜力的递送系统。
目的構建鮭魚降鈣素新型註射用溫度敏感原位凝膠繫統併對其膠凝特性和降血鈣效應進行評價。<br> 方法以泊洛沙姆 F127為主要基質材料,複閤使用泊洛沙姆 F68,製備鮭魚降鈣素註射用溫度敏感原位凝膠給藥繫統,以膠凝溫度、膠凝時間、流變學、質構特性為攷察指標,對該凝膠繫統性質進行評價;採用大鼠眼眶取血,鈣顯色法鑑測體內血清鈣離子濃度,對該凝膠繫統降血鈣效應進行研究。<br> 結果所製備的鮭魚降鈣素註射用溫度敏感原位凝膠的膠凝溫度為(35.3±1.3)℃,膠凝時間為(108.3±5.5)s,在25℃條件下為流動的液體,原位凝膠的黏度和黏滯力極低,方便註射給藥,噹溫度增至37℃時能夠迅速髮生相轉變,黏度和黏滯力等質構特性數據顯著增加,成為具有一定膠凝彊度的半固體;大鼠降血鈣效應結果顯示,該給藥繫統具有明顯的緩釋作用,其24 h 時血鈣濃度明顯低于普通註射劑組,相對于普通註射劑的藥理活性為138.6%。<br> 結論溫度敏感原位凝膠用于鮭魚降鈣素的註射給藥,是一種很有潛力的遞送繫統。
목적구건해어강개소신형주사용온도민감원위응효계통병대기효응특성화강혈개효응진행평개。<br> 방법이박락사모 F127위주요기질재료,복합사용박락사모 F68,제비해어강개소주사용온도민감원위응효급약계통,이효응온도、효응시간、류변학、질구특성위고찰지표,대해응효계통성질진행평개;채용대서안광취혈,개현색법감측체내혈청개리자농도,대해응효계통강혈개효응진행연구。<br> 결과소제비적해어강개소주사용온도민감원위응효적효응온도위(35.3±1.3)℃,효응시간위(108.3±5.5)s,재25℃조건하위류동적액체,원위응효적점도화점체력겁저,방편주사급약,당온도증지37℃시능구신속발생상전변,점도화점체력등질구특성수거현저증가,성위구유일정효응강도적반고체;대서강혈개효응결과현시,해급약계통구유명현적완석작용,기24 h 시혈개농도명현저우보통주사제조,상대우보통주사제적약리활성위138.6%。<br> 결론온도민감원위응효용우해어강개소적주사급약,시일충흔유잠력적체송계통。
Objective To prepare the thermosensitive in situ gel of salmon calcitonin for injection and evaluate the characteristics and hypocalcemic effect. <br> Methods Poloxamer F127 and poloxamer F68 were used to prepare the thermosensitive gel of samon calcitonin. The characteristics of the gel, such as gelation temperature, gelation time, rheological behavior and texture characteristics, were evaluated. Blood samples were drawn from orbit in rats, and coloration methods were used to monitor serum calcium ion concentration in order to study in vivo drug release and the hypocalcemic effect. <br> Results The gelation temperature of the salmon calcitonin-loaded in situ gel was (35.3 ± 1.3)℃, and the gelation time was (108.3 ± 5.5) s. The in situ gel, a fluid solution at 25 ℃, became semisolid quickly at 37 ℃ due to the fact the viscosity and mechanical parameters such as gel strength for gel was enhanced at 37℃. The in situ gel loading sCT clearly decreased serum calcium level in rats over a longer period of time as compared with the conventional injection indicating sustained characteristic in vivo, and produced 138.6%hypocalcemic efficacy relative to common injection. <br> Conclusion The thermosensitive in situ gel delivery system may be a promising candidate for injectable sustained delivery of salmon calcitonin.