Exploring the Potential of Anacardic Acid, its Natural and Synthetic Analogues, and Nanoformulations as a Potential Antibacterial Agent,including Multidrug-Resistant Bacteria: A Comprehensive Review

The increasing rise of multidrug-resistant bacteria necessitates an urgent need for the discovery of novel antibacterial agents. Natural products have long been a source for identifying and isolating novel antibacterial agents. Anacardic acids (AAs), a phenolic lipid isolated from solventextracted cashew nutshell liquid (CNSL) of Anacardium occidentale (Family Anacardiaceae), have garnered potential attention for their potent antibacterial properties. Besides Anacardium occidentale, different analogues of AAs have also been isolated from various natural sources. These natural and structurally optimized derivatives exhibited potential antibacterial properties against other bacterial strains. Although AAs are associated with a high level of antimicrobial activity against P. acnes, S. mutans, S. pyogenes, H. pylori, and methicillin-resistant S. aureus, their poor physicochemical properties are a major concern for their clinical translation. Encapsulating AAs in nanoformulations could be beneficial, as it can improve their poor pharmacokinetic properties, prevent enzymatic degradation during transport in the body, and facilitate site-specific release, thereby enhancing their therapeutic potential. Among the different nanocarriers studied, zein nanoparticles loaded with anacardic acid showed strong antibiofilm activity against E. faecalis, S. aureus, and P. aeruginosa. In contrast, the DNase-chitosan-coated solid lipid nanoparticles (Ana-SLNs-CH-DNase) demonstrated superior activity in disrupting mature S. aureus biofilms. Additionally, we have discussed the structure-activity relationship and mechanism of action of AAs, where it was found that AAs disrupt cell membrane functioning, inhibit bacterial respiration, quorum sensing, and cellular respiration, among other effects. These findings suggest that AAs and their analogues exhibit promising antibacterial activity, while nanoformulations offer a promising strategy to optimize their therapeutic potential.

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Journal
Mini-Reviews in Medicinal Chemistry
Published
2025-11-05
DOI
https://doi.org/10.2174/0113895575431411251009045624
Primary Topic
Ginkgo biloba and Cashew Applications
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article
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article

Exploring the Potential of Anacardic Acid, its Natural and Synthetic Analogues, and Nanoformulations as a Potential Antibacterial Agent,including Multidrug-Resistant Bacteria: A Comprehensive Review

Priyabrata Pattanayak, Ananya Pradhan
Mini-Reviews in Medicinal Chemistry
Ginkgo biloba and Cashew Applications
article

Exploring the Potential of Anacardic Acid, its Natural and Synthetic Analogues, and Nanoformulations as a Potential Antibacterial Agent,including Multidrug-Resistant Bacteria: A Comprehensive Review

Priyabrata Pattanayak, Ananya Pradhan
article en

Abstract

The increasing rise of multidrug-resistant bacteria necessitates an urgent need for the discovery of novel antibacterial agents. Natural products have long been a source for identifying and isolating novel antibacterial agents. Anacardic acids (AAs), a phenolic lipid isolated from solventextracted cashew nutshell liquid (CNSL) of Anacardium occidentale (Family Anacardiaceae), have garnered potential attention for their potent antibacterial properties. Besides Anacardium occidentale, different analogues of AAs have also been isolated from various natural sources. These natural and structurally optimized derivatives exhibited potential antibacterial properties against other bacterial strains. Although AAs are associated with a high level of antimicrobial activity against P. acnes, S. mutans, S. pyogenes, H. pylori, and methicillin-resistant S. aureus, their poor physicochemical properties are a major concern for their clinical translation. Encapsulating AAs in nanoformulations could be beneficial, as it can improve their poor pharmacokinetic properties, prevent enzymatic degradation during transport in the body, and facilitate site-specific release, thereby enhancing their therapeutic potential. Among the different nanocarriers studied, zein nanoparticles loaded with anacardic acid showed strong antibiofilm activity against E. faecalis, S. aureus, and P. aeruginosa. In contrast, the DNase-chitosan-coated solid lipid nanoparticles (Ana-SLNs-CH-DNase) demonstrated superior activity in disrupting mature S. aureus biofilms. Additionally, we have discussed the structure-activity relationship and mechanism of action of AAs, where it was found that AAs disrupt cell membrane functioning, inhibit bacterial respiration, quorum sensing, and cellular respiration, among other effects. These findings suggest that AAs and their analogues exhibit promising antibacterial activity, while nanoformulations offer a promising strategy to optimize their therapeutic potential.

Mini-Reviews in Medicinal ChemistryVol. 26
Siksha O Anusandhan University (IN)
Openalex Percentile: Top 49%
Ginkgo biloba and Cashew Applications
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