難溶性藥物姜黃素作為納米晶穩(wěn)定劑制備Pickering乳劑的研究
本文選題:姜黃素 切入點(diǎn):Pickering乳劑 出處:《中草藥》2017年09期
【摘要】:目的使用姜黃素納米晶(curcumin nanocrystalline,Cur-NC)作為固體顆粒穩(wěn)定劑,制備Cur-NC自穩(wěn)定Pickering乳劑(Cur-NC self-stabilized Pickering emulsion,Cur-NCSPE)。方法采用高壓均質(zhì)機(jī)制備Cur-NCSPE;比較不同的均質(zhì)壓力對(duì)Cur-NC粒徑的影響,考察Cur-NC的加入量對(duì)Cur-NCSPE形成的影響,用光學(xué)顯微鏡、掃描電子顯微鏡觀察乳劑的形態(tài)與結(jié)構(gòu),對(duì)Cur-NCSPE的穩(wěn)定性及體外藥物釋放進(jìn)行考察。結(jié)果隨著高壓均質(zhì)壓力的增加,Cur-NC的粒徑逐漸減小,當(dāng)高壓均質(zhì)壓力大于100 MPa后,Cur-NC的粒徑變化趨于平穩(wěn);隨著姜黃素(curcumin,Cur)投入量的增加,Cur-NC對(duì)油滴的包裹量增大,乳滴的粒徑逐漸減小,當(dāng)加入的藥物量能夠?qū)⒂偷瓮耆鼤r(shí),繼續(xù)增大藥物量對(duì)乳滴粒徑的影響不再明顯。Cur-NCSPE的穩(wěn)定性比Cur-NC和Cur高,Cur-NCSPE的體外釋放速率比Cur-NC和Cur的釋放速率顯著加快。結(jié)論成功制備了Cur-NCSPE,有望為中藥難溶性成分提供新的口服給藥技術(shù)平臺(tái)。
[Abstract]:Objective to prepare Cur-NC self-stable Pickering emulsion Cur-NC self-stabilized Pickering emulsionCur-NCSPEE using curcumin nanocrystalline Cur-NCas as solid particle stabilizer.Methods Cur-NCSPEs were prepared by high pressure homogenizer, the effect of different homogenization pressure on the particle size of Cur-NC was compared, the effect of Cur-NC addition on the formation of Cur-NCSPE was investigated, and the morphology and structure of emulsion were observed by optical microscope and scanning electron microscope.The stability of Cur-NCSPE and drug release in vitro were investigated.Results with the increase of high pressure homogenization pressure, the particle size of Cur-NC gradually decreased, when the pressure of high pressure was more than 100 MPa, the particle size of Cur-NC tended to be stable, and with the increase of the amount of curcumin (Curcumin Curn), the amount of oil droplet encapsulated by Cur-NC increased.The size of the emulsion droplets decreases gradually, and when the amount of the added drug is able to completely encapsulate the oil droplets,The stability of Cur-NCSPE was higher than that of Cur-NC and Cur. The release rate of Cur-NCSPE in vitro was significantly faster than that of Cur-NC and Cur.Conclusion Cur-NCSPEhas been successfully prepared, which is expected to provide a new platform for oral administration of insoluble components of traditional Chinese medicine.
【作者單位】: 重慶醫(yī)科大學(xué)藥學(xué)院重慶高校藥物工程研究中心;
【基金】:重慶市自然科學(xué)基金資助項(xiàng)目(cstc2016jcyjA0068)
【分類號(hào)】:R943
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