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Combined and targeted drugs delivery system for colorectal cancer treatment: Conatumumab decorated, reactive oxygen species sensitive irinotecan prodrug and quercetin co-loaded nanostructured lipid carriers.

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机构: [1]The Second Department of General Surgery, the Fourth Hospital of Hebei Medical University, Hebei Cancer Hospital, Shijiazhuang, Hebei Province, China. [2]Ward 1 of Department of Oncology, Shijiazhuang People's Hospital, Shijiazhuang, Hebei Province, China. [3]Ward 2 of Department of Oncology, Shijiazhuang People's Hospital, Shijiazhuang, Hebei Province, China. [4]Department of Endocrinology, the First Hospital of Xingtai, Xingtai, Hebei Province, China. [5]Department of Medical Oncology, the Fourth Hospital of Hebei Medical University, Hebei Cancer Hospital, Shijiazhuang, Hebei Province, China. [6]Department of Osteology, the First Hospital of Xingtai, Xingtai, Hebei Province, China.
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关键词: Colorectal cancer irinotecan prodrug lipid nanoparticles reactive oxygen species sensitive

摘要:
Colorectal cancer (CRC) is the third most frequently diagnosed cancer and this study aimed to develop a conatumumab decorated, irinotecan prodrug and quercetin co-loaded delivery system for combined and targeted colorectal cancer treatment.A conatumumab (C) decorated, irinotecan prodrug (I-p) and quercetin (Q) co-encapsulated NLC (C I-p/Q NLC) was developed. In vitro and in vivo antitumor efficiency of NLC was evaluated on CRC cells and mice xenograft.The results showed that the HT-29 cells uptake of C I-p/Q NLC was over 70%. Reactive oxygen species (ROS) sensitive irinotecan prodrug formulation showed improved drug release ability in hypoxic conditions. C I-p/Q NLC showed significantly higher cytotoxicity than non-decorated NLC, single drug-loaded NLC and free drugs. In vivo studies in a CRC-bearing model corroborated the capability of nanoparticles for the inhibition of cancer, leading to a reduction of tumor growth without systemic toxicity.The conatumumab decorated, ROS sensitive prodrug contained combination nano-system is a promising platform for CRC therapy.

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出版当年[2022]版:
大类 | 2 区 医学
小类 | 2 区 药学
最新[2025]版:
大类 | 2 区 医学
小类 | 1 区 药学
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出版当年[2022]版:
Q1 PHARMACOLOGY & PHARMACY
最新[2024]版:
Q1 PHARMACOLOGY & PHARMACY

影响因子: 最新[2024版] 最新五年平均 出版当年[2022版] 出版当年五年平均 出版前一年[2021版] 出版后一年[2023版]

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第一作者机构: [1]The Second Department of General Surgery, the Fourth Hospital of Hebei Medical University, Hebei Cancer Hospital, Shijiazhuang, Hebei Province, China.
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通讯机构: [5]Department of Medical Oncology, the Fourth Hospital of Hebei Medical University, Hebei Cancer Hospital, Shijiazhuang, Hebei Province, China. [6]Department of Osteology, the First Hospital of Xingtai, Xingtai, Hebei Province, China. [*1]Department of Medical Oncology, the Fourth Hospital of Hebei Medical University, Hebei Cancer Hospital, Shijiazhuang, Hebei Province, 050010, China [*2]Department of Osteology, the First Hospital of Xingtai, Xingtai, Hebei Province, 054001, China
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