Preparation and optimization of niosome encapsulated meropenem for significant antibacterial and anti-biofilm activity against methicillin-resistant Staphylococcus aureus isolates

An F1 formulation of niosome-encapsulated meropenem with a size of 51.3 ± 5.84 nm and an encapsulation efficiency of 84.86 ± 3.14 % was achieved. The synthesized niosomes prevented biofilm capacity with a biofilm growth inhibition index of 69 % and significantly downregulated <i>icaD, FnbA, Ebps</i>, and <i>Bap</i> gene expression in MRSA strains (p < 0.05). In addition, the F1 formulation increased antibacterial activity by 4-6 times compared with free meropenem. Interestingly, the F1 formulation of niosome-encapsulated meropenem indicated cell viability >90 % at all tested concentrations against normal HDF cells. The results of the present study indicate that niosome-encapsulated meropenem increased antibacterial and anti-biofilm activities without profound cytotoxicity in normal human cells, which could prove useful as a good drug delivery system.

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Publication Details

Journal
Heliyon
Published
2024-08-01
DOI
https://doi.org/10.1016/j.heliyon.2024.e35651
Citations
20
Primary Topic
Advancements in Transdermal Drug Delivery
Type
article
Field-Weighted Citation Impact
4.16

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article

Preparation and optimization of niosome encapsulated meropenem for significant antibacterial and anti-biofilm activity against methicillin-resistant Staphylococcus aureus isolates

Amir Mirzaie, Erfan Ghanbarzadeh, Kamal Paseban, Farnoush Falahi Robattorki et al.
20 citations
Heliyon
Advancements in Transdermal Drug Delivery
4.16
article

Preparation and optimization of niosome encapsulated meropenem for significant antibacterial and anti-biofilm activity against methicillin-resistant Staphylococcus aureus isolates

Amir Mirzaie, Erfan Ghanbarzadeh, Kamal Paseban, Farnoush Falahi Robattorki, Romina Andalibi, Arezou Azari, Abbas Haddadian, Aliasghar Bagheri Kashtali, Hedieh Dibah, Reza Amani, Arman Chitgarzadeh, Tohid Piri Gharaghie, Shadi Hajrasouiha, Tina Rashidian, Zahra Pirdolat, Massoumeh Salarkia, Dorsa Sadat Shahrava, Fatemeh Safaeinikjoo, Sama Noroozi, Niloofar Saeinia, Ali Ahmadiyan, Roza Mazid Abadi, Rokhshad Gharehcheloo, Fatima Sabouri, Faezeh Sadat Kermani, Niusha Sadat Hosseini, Atena Seifi, Aryan Aryan Tavana
article en
20 citations

Abstract

An F1 formulation of niosome-encapsulated meropenem with a size of 51.3 ± 5.84 nm and an encapsulation efficiency of 84.86 ± 3.14 % was achieved. The synthesized niosomes prevented biofilm capacity with a biofilm growth inhibition index of 69 % and significantly downregulated <i>icaD, FnbA, Ebps</i>, and <i>Bap</i> gene expression in MRSA strains (p < 0.05). In addition, the F1 formulation increased antibacterial activity by 4-6 times compared with free meropenem. Interestingly, the F1 formulation of niosome-encapsulated meropenem indicated cell viability >90 % at all tested concentrations against normal HDF cells. The results of the present study indicate that niosome-encapsulated meropenem increased antibacterial and anti-biofilm activities without profound cytotoxicity in normal human cells, which could prove useful as a good drug delivery system.

HeliyonVol. 10(16)
Islamic Azad University Roudehen Branch (IR), Islamic Azad University of Zanjan (IR), Islamic Azad University South Tehran Branch (IR), Tarbiat Modares University (IR), Islamic Azad University, Science and Research Branch (IR), Guilan University of Medical Sciences (IR), University of Utah (US), Islamic Azad University of Parand (IR), Biotechnology Research Center (IR), Islamic Azad University of Shahrekord (IR), Islamic Azad University Pharmaceutical Sciences Branch (IR)
Islamic Azad University, Ahar Branch, Islamic Azad University of Shahrekord, Islamic Azad University, Islamic Azad University, Shahrekord
Openalex Percentile: Top 5%
Advancements in Transdermal Drug Delivery
4.16
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