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The Clinical Application of Tumor Treating Fields Therapy in Glioblastoma
Published on: April 16, 2019
Transforming stealthy to sticky nanocarriers: a potential application for tumor therapy
Alidha Gafur1, Natalia Kristi1, Ali Maruf1
1Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing, 400030, China. yzybio@cqu.edu.cn.
Abstract:
Nanomedicine has shown remarkable progress in preclinical studies of tumor treatment. Over the past decade, scientists have developed various nanocarriers (NCs) for delivering drugs into the tumor area. However, the average amount of accumulated drugs in tumor sites is far from satisfactory. This limitation is strongly related to the corona formation during blood circulation. To overcome this issue, NCs should be designed to become highly stealthy by modifying their surface charge. However, at the same time, stealthy effects not only prevent protein formation but also alleviate the cellular uptake of NCs. Therefore, it is necessary to develop NCs with switchable properties, which are stealthy in the circulation system and sticky when arriving at tumor sites. In this review, we discuss the recent strategies to develop passive and active charge-switchable NCs, known as chameleon-like drug delivery systems, which can reversibly transform their surface from stealthy to sticky and have various designs.
Insights
Scientists are developing "chameleon-like" nanocarriers for improved tumor drug delivery. These systems switch from stealthy to sticky, enhancing drug accumulation at tumor sites by overcoming circulation challenges.
Area of Science:
- Nanomedicine
- Biotechnology
- Drug Delivery Systems
Background:
- Nanomedicine shows promise in preclinical tumor treatment, utilizing nanocarriers (NCs) for drug delivery.
- Current NCs face limitations in tumor drug accumulation due to protein corona formation during circulation.
- Stealth properties, while preventing protein formation, also reduce cellular uptake, necessitating adaptable NC designs.
Purpose of the Study:
- To review strategies for developing charge-switchable nanocarriers for enhanced tumor drug delivery.
- To explore "chameleon-like" drug delivery systems with reversible surface properties.
- To address the challenge of insufficient drug accumulation in tumor sites.
Main Methods:
- Discussion of recent strategies for passive and active charge-switchable nanocarriers.
- Analysis of nanocarrier designs that exhibit reversible surface transformations.
- Focus on overcoming limitations posed by protein corona formation and cellular uptake.
Main Results:
- Development of nanocarriers with switchable surface properties is crucial for effective tumor targeting.
- Charge-switchable NCs can transition from stealthy to sticky states, improving tumor site accumulation.
- These "chameleon-like" systems offer a promising approach to enhance nanomedicine efficacy.
Conclusions:
- Charge-switchable nanocarriers represent a significant advancement in overcoming drug delivery barriers.
- Reversible surface modification of NCs is key to achieving targeted drug delivery in cancer therapy.
- Future nanomedicine designs should incorporate switchable properties for optimized therapeutic outcomes.
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