Related Experiment Video
Updated: Sep 29, 2025

Viral Nanoparticles for In vivo Tumor Imaging
Published on: November 16, 2012
Bioinspired soft nanovesicles for site-selective cancer imaging and targeted therapies
Rajendra Prasad1, João Conde1,2
1NOVA Medical School, Faculdade de Ciências Médicas, Universidade Nova de Lisboa, Lisbon, Portugal.
Abstract:
Cell-to-cell communication within the heterogeneous solid tumor environment plays a significant role in the uncontrolled metastasis of cancer. To inhibit the metastasis and growth of cancer cells, various chemically designed and biologically derived nanosized biomaterials have been applied for targeted cancer therapeutics applications. Over the years, bioinspired soft nanovesicles have gained tremendous attention for targeted cancer therapeutics due to their easy binding with tumor microenvironment, natural targeting ability, bio-responsive nature, better biocompatibility, high cargo capacity for multiple therapeutics agents, and long circulation time. These cell-derived nanovesicles guard their loaded cargo molecules from immune clearance and make them site-selective to cancer cells due to their natural binding and delivery abilities. Furthermore, bioinspired soft nanovesicles prevent cell-to-cell communication and secretion of cancer cell markers by delivering the therapeutics agents predominantly. Cell-derived vesicles, namely, exosomes, extracellular vesicles, and so forth have been recognized as versatile carriers for therapeutic biomolecules. However, low product yield, poor reproducibility, and uncontrolled particle size distribution have remained as major challenges of these soft nanovesicles. Furthermore, the surface biomarkers and molecular contents of these vesicles change with respect to the stage of disease and types. Here in this review, we have discussed numerous examples of bioinspired soft vesicles for targeted imaging and cancer therapeutic applications with their advantages and limitations. Importance of bioengineered soft nanovesicles for localized therapies with their clinical relevance has also been addressed in this article. Overall, cell-derived nanovesicles could be considered as clinically relevant platforms for cancer therapeutics. This article is categorized under: Biology-Inspired Nanomaterials > Nucleic Acid-Based Structures Therapeutic Approaches and Drug Discovery > Nanomedicine for Oncologic Disease.
Insights
Bioinspired soft nanovesicles show promise for targeted cancer therapeutics by inhibiting metastasis. These cell-derived vesicles offer natural targeting and biocompatibility, though challenges in production and standardization remain for clinical use.
Area of Science:
- Nanomedicine
- Oncologic Disease
- Biology-Inspired Nanomaterials
Background:
- Solid tumors utilize cell-to-cell communication for metastasis.
- Nanosized biomaterials are explored for targeted cancer therapeutics.
- Bioinspired soft nanovesicles offer unique advantages for cancer treatment.
Purpose of the Study:
- To review bioinspired soft vesicles for targeted cancer imaging and therapeutics.
- To discuss the advantages and limitations of these nanovesicles.
- To highlight the clinical relevance of bioengineered nanovesicles for localized therapies.
Main Methods:
- Review of existing literature on bioinspired soft nanovesicles.
- Discussion of examples for targeted imaging and cancer therapeutics.
- Analysis of advantages, limitations, and clinical relevance.
Main Results:
- Bioinspired soft nanovesicles demonstrate natural targeting, biocompatibility, and high cargo capacity.
- These vesicles can inhibit cancer cell communication and metastasis.
- Challenges include low yield, reproducibility, and particle size control.
Conclusions:
- Cell-derived nanovesicles, like exosomes, are versatile carriers for therapeutic biomolecules.
- Bioengineered soft nanovesicles represent a clinically relevant platform for cancer therapeutics.
- Further research is needed to overcome production challenges for widespread clinical application.

