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Updated: Oct 2, 2025

A "Plug-And-Display" Nanoparticle Vaccine Platform Based on Outer Membrane Vesicles Displaying SARS-CoV-2 Receptor-Binding Domain
Published on: July 25, 2022
Outer membrane vesicles as biomimetic vaccine carriers against infections and cancers
Nur Najihah Izzati Mat Rani1,2, Zahraa M Alzubaidi1, Adeel Masood Butt3
1Centre for Drug Delivery Technology, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, Kuala Lumpur, Malaysia.
Abstract:
In the last decade, nanoparticle-based therapeutic modalities have emerged as promising treatment options for cancer and infectious diseases. To improve prognosis, chemotherapeutic and antimicrobial drugs must be delivered selectively to the target sites. Researchers have increasingly focused their efforts on improving drug delivery, with a particular emphasis on cancer and infectious diseases. When drugs are administered systemically, they become diluted and can diffuse to all tissues but only until the immune system intervenes and quickly removes them from circulation. To enhance and prolong the systemic circulation of drugs, nanocarriers have been explored and used; however, nanocarriers have a major drawback in that they can trigger immune responses. Numerous nanocarriers for optimal drug delivery have been developed using innovative and effective biointerface technologies. Autologous cell-derived drug carriers, such as outer membrane vesicles (OMVs), have demonstrated improved bioavailability and reduced toxicity. Thus, this study investigates the use of biomimetic OMVs as biomimetic vaccine carriers against infections and cancers to improve our understanding in the field of nanotechnology. In addition, discussion on the advantages, disadvantages, and future prospects of OMVs will also be explored. This article is categorized under: Therapeutic Approaches and Drug Discovery > Nanomedicine for Oncologic Disease Therapeutic Approaches and Drug Discovery > Nanomedicine for Infectious Disease Biology-Inspired Nanomaterials > Protein and Virus-Based Structures.
Insights
Biomimetic outer membrane vesicles (OMVs) show promise as drug delivery nanocarriers for cancer and infectious diseases. These cell-derived vesicles offer improved bioavailability and reduced toxicity compared to traditional nanocarriers.
Area of Science:
- Nanotechnology
- Nanomedicine
- Biomaterials
Background:
- Nanoparticle-based therapies are emerging for cancer and infectious diseases.
- Selective drug delivery is crucial for improving therapeutic outcomes.
- Conventional nanocarriers can trigger immune responses and have limited circulation time.
Purpose of the Study:
- To investigate biomimetic outer membrane vesicles (OMVs) as vaccine carriers.
- To explore OMVs for targeted delivery against infections and cancers.
- To enhance understanding of nanotechnology in disease treatment.
Main Methods:
- Utilizing autologous cell-derived drug carriers, specifically outer membrane vesicles (OMVs).
- Developing innovative biointerface technologies for nanocarrier optimization.
- Investigating biomimetic OMVs for enhanced bioavailability and reduced toxicity.
Main Results:
- Autologous cell-derived OMVs demonstrate improved bioavailability.
- OMVs show potential for reduced toxicity in drug delivery.
- Biomimetic OMVs are explored as effective carriers for therapeutic applications.
Conclusions:
- Biomimetic OMVs represent a promising advancement in nanomedicine.
- OMVs offer advantages over traditional nanocarriers for treating cancer and infectious diseases.
- Further research into OMVs' advantages, disadvantages, and future prospects is warranted.
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