Herceptin-decorated paclitaxel-loaded poly(lactide-co-glycolide) nanobubbles: Ultrasound-facilitated release and targeted accumulation in breast cancers
Herceptin-decorated paclitaxel-loaded poly(lactide-co-glycolide) nanobubbles: Ultrasound-facilitated release and targeted accumulation in breast cancers
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赫赛汀修饰的紫杉醇负载聚丙交酯乙交酯纳米气泡:超声促进释放和乳腺癌中的靶向积累
DOI:
10.1080/10837450.2019.1709500
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发表时间:
2019-12
影响因子:
3.4
通讯作者:
Jie Luo
中科院分区:
文献类型:
--
作者:
Shigen Zhong;Zhiyu Ling;Zhiyi Zhou;Jing He;Haitao Ran;Zhigang Wang;Qunxia Zhang;Weixiang Song;Yong Zhang;Jie Luo
Ultrasound can promote the drug release from drug-loaded substances and alter the tumor local microenvironment to facilitate the transport of drug carriers into the tumor tissues. Based on the altered tumor microenvironment, nanobubbles (NBs) as drug carriers with surfaces functionalized with targeting ligands can reach the tumor sites, thereby increasing the efficacy of chemotherapy. Herein,paclitaxel (PTX)-loaded poly(lactide-co-glycolide) (PLGA) NBs are prepared as drug carriers with covalently conjugated herceptin (anti-HER2 monoclonal antibody) on the surface to guide the target. The effect of ultrasound on the drug release and targeting of the herceptin-conjugated drug-loaded nanobubbles (PTXNBs-HER) on the cancerous cells is determined. The use of ultrasound significantly improves the cell targeting capability in vitro and efficiency of enhanced permeability and retention in vivo. The combination of PTX-NBs-HER and ultrasound facilitates the release of PTX, as well as the uptake and cell apoptosis in vitro. The in vivo application of both PTX-NBs-HER and ultrasound enhances the PTX targeting and accumulation in breast cancers while reducing the transmission and distribution of PTX in healthy organs. The combination of ultrasound with PTX-NBs-HER as contrast agents and drug carriers affords an image-guided drug delivery system for the precise targeted therapy of tumors.
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影响因子:
3.8
作者:
Wu ST;Fowler AJ;Garmon CB;Fessler AB;Ogle JD;Grover KR;Allen BC;Williams CD;Zhou R;Yazdanifar M;Ogle CA;Mukherjee P
通讯作者:
Mukherjee P
影响因子:
3.5
作者:
Hussein F;Antonescu C;Karshafian R
通讯作者:
Karshafian R
影响因子:
6
作者:
Kumar, Rishikesh;Sahoo, Ganesh Chandra;Das, Pradeep
通讯作者:
Das, Pradeep
影响因子:
12.4
作者:
Li W;Hou W;Guo X;Luo L;Li Q;Zhu C;Yang J;Zhu J;Du Y;You J
通讯作者:
You J
影响因子:
3.8
作者:
Müller V;Clemens M;Jassem J;Al-Sakaff N;Auclair P;Nüesch E;Holloway D;Shing M;Bang YJ
通讯作者:
Bang YJ