Ultrasonically controlled albumin-conjugated liposomes for breast cancer therapy

被引:37
作者
Awad, Nahid S. [1 ]
Paul, Vinod [1 ]
Al-Sayah, Mohammad H. [2 ,3 ]
Husseini, Ghaleb A. [1 ,3 ]
机构
[1] Amer Univ Sharjah, Dept Chem Engn, Sharjah, U Arab Emirates
[2] Amer Univ Sharjah, Dept Biol Chem & Environm Sci, Sharjah, U Arab Emirates
[3] Amer Univ Sharjah, Biosci & Bioengn Res Inst, Sharjah, U Arab Emirates
关键词
Human serum albumin; liposomes; calcein; breast cancer; ultrasound; DRUG-DELIVERY; STEALTH LIPOSOMES; CELLULAR UPTAKE; RELEASE; ULTRASOUND; NANOPARTICLES; ENDOCYTOSIS; SONOPORATION; DOXORUBICIN; PRINCIPLES;
D O I
10.1080/21691401.2019.1573175
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Targeted liposomes have high potentials in the specific and effective delivery of their loaded therapeutic agents to the tumour site. Once at the tumour site, it is important that these liposomes are triggered to release their load in a controlled and effective manner. In this study, pegylated (stealth) liposomes conjugated to human serum albumin (HSA) were investigated for the delivery of a model drug (calcein) to breast cancer cells. The fluorescent results showed that calcein uptake by the two breast cancer cell lines (MDA-MB-231 and MCF-7) was significantly higher with the HSA-PEG liposomes compared to the non-targeted control liposomes. Furthermore, the exposure to low-frequency ultrasound (LFUS) resulted in a statistically significant uptake of calcein compared to the uptake without ultrasound. The described drug delivery (DD) system, which involves combining the targeted liposomal formulation with ultrasonic triggering techniques, promises a safe, effective and site-specific breast cancer therapy.
引用
收藏
页码:705 / 714
页数:10
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