高校化学工程学报
高校化學工程學報
고교화학공정학보
JOURNAL OF CHEMICAL ENGINEERING OF CHINESE UNIVERSITIES
2014年
3期
648-653
,共6页
吴洁%丁师杰%陈静%刘超%黄娟娟
吳潔%丁師傑%陳靜%劉超%黃娟娟
오길%정사걸%진정%류초%황연연
凹凸棒粘土%海藻酸钠%复合微球%缓释
凹凸棒粘土%海藻痠鈉%複閤微毬%緩釋
요철봉점토%해조산납%복합미구%완석
Attapulgite (ATP)%sodium alginate%sustained release%chitosan
将凹凸棒黏土(ATP)与海藻酸钠(SA)进行复合以改善SA的缓释性能。以ATP/SA复合物为球芯材料,壳聚糖(CS)为包覆材料,采用复凝聚法制备凹土/海藻酸钠/壳聚糖复合微球(ASCM),并以双氯芬酸钠(DS)为模型药物,考察了凹土添加量对复合微球溶胀性能、载药性能和缓释性能的影响。结果表明,凹土的加入改善了微球的溶胀性能和缓释性能,而对微球载药性能影响不大。与海藻酸钠/壳聚糖微球(SCM)相比,当复合微球中ATP/SA(w/w)为20%时,其在pH6.8的磷酸缓冲溶液中2 h的累积释放率由58.8%减小到38.7%。复合微球体外释放动力学数据表明,其释药行为可以很好地用一级动力学方程拟合。凹土的加入有效改善了SA的缓释性能,ASCM可作为缓释药物的载体材料。
將凹凸棒黏土(ATP)與海藻痠鈉(SA)進行複閤以改善SA的緩釋性能。以ATP/SA複閤物為毬芯材料,殼聚糖(CS)為包覆材料,採用複凝聚法製備凹土/海藻痠鈉/殼聚糖複閤微毬(ASCM),併以雙氯芬痠鈉(DS)為模型藥物,攷察瞭凹土添加量對複閤微毬溶脹性能、載藥性能和緩釋性能的影響。結果錶明,凹土的加入改善瞭微毬的溶脹性能和緩釋性能,而對微毬載藥性能影響不大。與海藻痠鈉/殼聚糖微毬(SCM)相比,噹複閤微毬中ATP/SA(w/w)為20%時,其在pH6.8的燐痠緩遲溶液中2 h的纍積釋放率由58.8%減小到38.7%。複閤微毬體外釋放動力學數據錶明,其釋藥行為可以很好地用一級動力學方程擬閤。凹土的加入有效改善瞭SA的緩釋性能,ASCM可作為緩釋藥物的載體材料。
장요철봉점토(ATP)여해조산납(SA)진행복합이개선SA적완석성능。이ATP/SA복합물위구심재료,각취당(CS)위포복재료,채용복응취법제비요토/해조산납/각취당복합미구(ASCM),병이쌍록분산납(DS)위모형약물,고찰료요토첨가량대복합미구용창성능、재약성능화완석성능적영향。결과표명,요토적가입개선료미구적용창성능화완석성능,이대미구재약성능영향불대。여해조산납/각취당미구(SCM)상비,당복합미구중ATP/SA(w/w)위20%시,기재pH6.8적린산완충용액중2 h적루적석방솔유58.8%감소도38.7%。복합미구체외석방동역학수거표명,기석약행위가이흔호지용일급동역학방정의합。요토적가입유효개선료SA적완석성능,ASCM가작위완석약물적재체재료。
Attapulgite (ATP) was composited with sodium alginate (SA) to improve the sustained release properties of SA. Attapulgite/sodium alginate/chitosan composite microspheres (ASCM) were prepared by complex coacervation using ATP/SA composites as the core material of the microspheres and chitosan (CS) as the coating material. The effects of ATP on swelling, drug loading and sustained release of ASCM were investigated with diclofenac sodium (DS) as a model drug, and the optimum amount of ATP were obtained. The results show that ASCM exhibits excellent swelling and sustained release ability. Compared with sodium alginate/chitosan microspheres (SCM), the cumulative release of DS from ASCM (20 %(wt) ATP/SA (w/w)) decreased from 58.8% to 38.7% after 2 h in phosphate buffer solution at pH 6.8. The study of drug release kinetics shows that the releasing processes are better fitted by first-order release kinetic model. The incorporation of ATP in microspheres improves the releasing performance of SA, and ASCM can be used as a potential sustained release carrier.