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Recent Advancements in Stimuli Responsive Drug Delivery Platforms for Active and Passive Cancer Targeting
Muhammad Abdur Rahim1, Nasrullah Jan1, Safiullah Khan1
1Department of Pharmaceutics, Faculty of Pharmacy, The Islamia University of Bahawalpur, Bahawalpur 63100, Punjab, Pakistan.
Abstract:
The tumor-specific targeting of chemotherapeutic agents for specific necrosis of cancer cells without affecting the normal cells poses a great challenge for researchers and scientists. Though extensive research has been carried out to investigate chemotherapy-based targeted drug delivery, the identification of the most promising strategy capable of bypassing non-specific cytotoxicity is still a major concern. Recent advancements in the arena of onco-targeted therapies have enabled safe and effective tumor-specific localization through stimuli-responsive drug delivery systems. Owing to their promising characteristic features, stimuli-responsive drug delivery platforms have revolutionized the chemotherapy-based treatments with added benefits of enhanced bioavailability and selective cytotoxicity of cancer cells compared to the conventional modalities. The insensitivity of stimuli-responsive drug delivery platforms when exposed to normal cells prevents the release of cytotoxic drugs into the normal cells and therefore alleviates the off-target events associated with chemotherapy. Contrastingly, they showed amplified sensitivity and triggered release of chemotherapeutic payload when internalized into the tumor microenvironment causing maximum cytotoxic responses and the induction of cancer cell necrosis. This review focuses on the physical stimuli-responsive drug delivery systems and chemical stimuli-responsive drug delivery systems for triggered cancer chemotherapy through active and/or passive targeting. Moreover, the review also provided a brief insight into the molecular dynamic simulations associated with stimuli-based tumor targeting.
Insights
Stimuli-responsive drug delivery systems offer targeted chemotherapy, selectively destroying cancer cells while sparing normal cells. These advanced platforms enhance drug efficacy and minimize side effects for improved cancer treatment.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Targeted chemotherapy faces challenges in selectively eliminating cancer cells without harming healthy tissues.
- Non-specific cytotoxicity remains a significant concern in conventional chemotherapy.
- Stimuli-responsive drug delivery systems represent a promising advancement in onco-targeted therapies.
Purpose of the Study:
- To review physical and chemical stimuli-responsive drug delivery systems for triggered cancer chemotherapy.
- To explore the mechanisms of active and passive targeting in these systems.
- To provide insights into molecular dynamic simulations for stimuli-based tumor targeting.
Main Methods:
- Review of current literature on stimuli-responsive drug delivery systems.
- Analysis of physical and chemical stimuli triggers for drug release.
- Discussion of targeting strategies (active and passive) and their integration.
- Inclusion of molecular dynamic simulation approaches for system design.
Main Results:
- Stimuli-responsive platforms demonstrate enhanced bioavailability and selective cancer cell cytotoxicity.
- These systems prevent drug release in normal cells, mitigating off-target effects.
- Triggered drug release within the tumor microenvironment maximizes cytotoxic response and necrosis induction.
Conclusions:
- Stimuli-responsive drug delivery systems offer a revolutionary approach to chemotherapy, improving efficacy and safety.
- These platforms hold significant potential for overcoming the limitations of conventional cancer treatments.
- Further research, including molecular dynamics, can optimize stimuli-responsive systems for clinical application.
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