文獻:AIE-Featured Redox-Sensitive Micelles for Bioimaging and Efficient Anticancer Drug Delivery
作者:by Wei Zhao 1,?,Zixue Li 1,?,Na Liang 2,*,Jiyang Liu 1,Pengfei Yan 1 andShaoping Sun
文獻鏈接:https://www.mdpi.com/1422-0067/23/18/10801
The drug-loaded Bi(mPEG-S-S)-TPE micelles were obtained as follows. At first, the Bi(mPEG-S-S)-TPE dispersion in distilled water was prepared. Then, the PTX in the acetone solution was added. After being sonicated for 3 min (on for 3 s and off for 2 s), the mixture was dialyzed (MWCO of 3500 Da) against distilled water for 2 h and further filtrated with a 0.45 μm filter to obtain the drug-loaded micelles. The micelles could be further freeze-dried and stored as a white powder.
XRD analysis was used to analyze the crystalline characteristic of PTX in the micelles (Geigerflex, Rigaku Co., Tokyo, Japan). Data were collected from 5° to 50° with a step-scan mode. The dynamic light-scattering method was employed to determine the particle size and zeta potential of PTX-loaded micelles (Zetasizer Nano-ZS90, Malvern Instruments, Malvern, UK). The drug loading (DL) and encapsulation efficiency (EE) were calculated using Equations (2) and (3), respectively.
Bi(mPEG-S-S)-TPE膠束的制備與表征
載藥的Bi(mPEG-S-S)-TPE膠束如下獲得。首先,制備了Bi(mPEG-S-S)-TPE在蒸餾水中的分散體。然后,加入丙酮溶液中的PTX。經過3分鐘的超聲處理(開啟3秒,關閉2秒)后,將混合物用蒸餾水透析(MWCO為3500 Da)2小時,然后用0.45μm過濾器進一步過濾,得到載藥膠束。膠束可以進一步冷凍干燥,并以白色粉末的形式儲存。
XRD分析用于分析膠束中PTX的結晶特性。采用階躍掃描模式從5°到50°收集數據。采用動態光散射法測定PTX負載膠束的粒徑和ζ電位(Zetasizer Nano-ZS90,Malvern Instruments,英國Malvern)。分別使用方程式(2)和(3)計算藥物負載量(DL)和包封效率(EE)。
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