TY - JOUR
T1 - Outer membrane vesicles as biomimetic vaccine carriers against infections and cancers
AU - Mat Rani, Nur Najihah Izzati
AU - Alzubaidi, Zahraa M.
AU - Butt, Adeel Masood
AU - Mohammad Faizal, Nur Dini Fatini
AU - Sekar, Mahendran
AU - Azhari, Hanisah
AU - Mohd Amin, Mohd Cairul Iqbal
N1 - Funding Information:
The authors are thankful to the Universiti Kebangsaan Malaysia, Faculty of Pharmacy, Kuala Lumpur Campus, and Faculty of Pharmacy & Health Sciences, Universiti Kuala Lumpur Royal College of Medicine (UniKL RCMP), for providing the necessary facilities to carry out this work. The figures in this review article were created using BioRender.com.
Publisher Copyright:
© 2022 Wiley Periodicals LLC.
PY - 2022/7
Y1 - 2022/7
N2 - 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.
AB - 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.
KW - biomimetics
KW - cancer
KW - drug delivery
KW - infections
KW - OMVs
KW - vaccines
UR - http://www.scopus.com/inward/record.url?scp=85125107885&partnerID=8YFLogxK
U2 - 10.1002/wnan.1784
DO - 10.1002/wnan.1784
M3 - Review Article
C2 - 35194964
AN - SCOPUS:85125107885
SN - 1939-5116
VL - 14
JO - WIREs Nanomedicine and Nanobiotechnology
JF - WIREs Nanomedicine and Nanobiotechnology
IS - 4
M1 - e1784
ER -