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A Flow Cytometry-Based Cell Surface Protein Binding Assay for Assessing Selectivity and Specificity of an Anticancer Aptamer
Published on: September 13, 2022
Cancer targeted therapeutics: From molecules to drug delivery vehicles
1Department of Biomedical Engineering, The City College of New York, New York, NY 10031, United States.
Abstract:
The pitfall of all chemotherapeutics lies in drug resistance and the severe side effects experienced by patients. One way to reduce the off-target effects of chemotherapy on healthy tissues is to alter the biodistribution of drug. This can be achieved in two ways: Passive targeting utilizes shape, size, and surface chemistry to increase particle circulation and tumor accumulation. Active targeting employs either chemical moieties (e.g. peptides, sugars, aptamers, antibodies) to selectively bind to cell membranes or responsive elements (e.g. ultrasound, magnetism, light) to deliver its cargo within a local region. This article will focus on the systemic administration of anti-cancer agents and their ability to home to tumors and, if relevant, distant metastatic sites.
Insights
Chemotherapy faces challenges with drug resistance and side effects. This review explores methods to improve anti-cancer drug delivery, focusing on passive and active targeting strategies to enhance tumor accumulation and reduce off-target toxicity.
Area of Science:
- Oncology
- Nanomedicine
- Drug Delivery
Background:
- Chemotherapeutics are limited by drug resistance and severe side effects.
- Off-target toxicity to healthy tissues is a major concern in chemotherapy.
- Altering drug biodistribution is key to improving treatment efficacy and patient outcomes.
Purpose of the Study:
- To review strategies for enhancing the tumor-homing ability of systemically administered anti-cancer agents.
- To discuss passive and active targeting methods for improved drug delivery.
- To highlight the potential of these strategies in treating primary tumors and distant metastases.
Main Methods:
- Review of passive targeting strategies based on particle characteristics (size, shape, surface chemistry).
- Exploration of active targeting mechanisms utilizing chemical moieties or responsive elements for selective drug delivery.
- Focus on systemic administration routes for anti-cancer agents.
Main Results:
- Passive targeting enhances drug circulation time and tumor accumulation.
- Active targeting enables selective binding to cancer cells or localized drug release.
- Both strategies show promise for improving drug delivery to tumors and metastatic sites.
Conclusions:
- Targeted drug delivery systems offer a promising approach to overcome chemotherapy limitations.
- Optimizing biodistribution can significantly reduce side effects and combat drug resistance.
- Further research into advanced targeting strategies is crucial for effective cancer treatment.
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