{"id":3371,"date":"2026-08-06T00:00:00","date_gmt":"2026-08-06T00:00:00","guid":{"rendered":"https:\/\/futurenews24.com\/index.php\/2026\/08\/06\/s41598-026-63745-z\/"},"modified":"2026-08-06T12:59:09","modified_gmt":"2026-08-06T12:59:09","slug":"s41598-026-63745-z","status":"publish","type":"post","link":"https:\/\/futurenews24.com\/index.php\/2026\/08\/06\/s41598-026-63745-z\/","title":{"rendered":"Piperazine linked chitosan schiff base nanoparticles as a novel antibiofilm and antibacterial technique towards clinically related pathogens"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div id=\"\">\n<p class=\"c-article-references__text\" id=\"ref-CR1\">Ullah, S. et al. Mechanistic insights and therapeutic improvements in engineered nanomaterial-driven disruption of biofilm dynamics. 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Article\u00a0 CAS\u00a0 PubMed\u00a0 [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":3373,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"fifu_image_url":"https:\/\/media.springernature.com\/m685\/springer-static\/image\/art%3A10.1038%2Fs41598-026-63745-z\/MediaObjects\/41598_2026_63745_Fig1_HTML.png","fifu_image_alt":"","jnews-multi-image_gallery":[],"jnews_single_post":[],"jnews_primary_category":[],"jnews_override_bookmark_settings":[],"jnews_social_meta":[],"jnews_override_counter":[],"footnotes":""},"categories":[10],"tags":[1694,3758,799,2599,3759,1720,2600,3761,3756,3760,3757,28],"class_list":["post-3371","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-biotechnology","tag-antibacterial","tag-antibiofilm","tag-base","tag-chitosan","tag-clinically","tag-linked","tag-nanoparticles","tag-pathogens","tag-piperazine","tag-relevant","tag-schiff","tag-strategy"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Piperazine linked chitosan schiff base nanoparticles as a novel antibiofilm and antibacterial technique towards clinically related pathogens - Future News 24<\/title>\n<meta name=\"description\" content=\"The development of multifunctional antimicrobial materials capable of targeting both planktonic bacteria and biofilm-associated infections remains a critical challenge in combating antimicrobial resistance. In this study, a novel piperazine-linked chitosan Schiff base (Cs-TPA-PiP) and its ionically crosslinked nanoparticle formulation (Cs-TPA-PiP NPs) were synthesized and structurally characterized. The antimicrobial potential of both Cs-TPA-PiP and Cs-TPA-PiP NPs was evaluated against a panel of nine standard clinically significant bacterial strains. The compounds demonstrated significant and broad-spectrum antibacterial activity. The minimum inhibitory concentration (MIC) values demonstrated potent efficacy, with Cs-TPA-PiP and its Cs-TPA-PiP NPs ranging from 0.63 to 2.50&amp;nbsp;mg\/mL and 1.00&#8211;5.00&amp;nbsp;mg\/mL, respectively. Notably, both agents exhibited a strong dose-dependent inhibitory effect on biofilm formation. While Cs-TPA-PiP showed lower MIC values against planktonic cells, the corresponding Cs-TPA-PiP NPs with an ultra-small spherical size of 15.6&amp;nbsp;nm exhibited superior antibiofilm performance, ranging from 73.00% to 95.00% inhibition of biofilm biomass at 1&#215; MIC in strong biofilm-producing strains. Transmission electron microscopy (TEM) confirmed severe morphological alterations and membrane disruption in treated bacterial cells, consistent with a membrane-targeting mechanism. In silico molecular docking studies suggested that the compound has favorable binding affinity for the critical bacterial cell wall target, Sortase A, thereby identifying it as a potential theoretical target requiring further validation. Our findings collectively establish Cs-TPA-PiP and its Cs-TPA-PiP NPs as effective antibacterial and anti-biofilm candidates, with their activity primarily attributed to membrane disruption. The proposed role of Sortase A inhibition remains hypothetical and warrants further investigation. These findings highlight their potential as multifunctional antibacterial platforms for managing biofilm-associated and resistant bacterial infections.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/futurenews24.com\/index.php\/2026\/08\/06\/s41598-026-63745-z\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Piperazine linked chitosan schiff base nanoparticles as a novel antibiofilm and antibacterial technique towards clinically related pathogens - Future News 24\" \/>\n<meta property=\"og:description\" content=\"The development of multifunctional antimicrobial materials capable of targeting both planktonic bacteria and biofilm-associated infections remains a critical challenge in combating antimicrobial resistance. In this study, a novel piperazine-linked chitosan Schiff base (Cs-TPA-PiP) and its ionically crosslinked nanoparticle formulation (Cs-TPA-PiP NPs) were synthesized and structurally characterized. The antimicrobial potential of both Cs-TPA-PiP and Cs-TPA-PiP NPs was evaluated against a panel of nine standard clinically significant bacterial strains. The compounds demonstrated significant and broad-spectrum antibacterial activity. The minimum inhibitory concentration (MIC) values demonstrated potent efficacy, with Cs-TPA-PiP and its Cs-TPA-PiP NPs ranging from 0.63 to 2.50&amp;nbsp;mg\/mL and 1.00&#8211;5.00&amp;nbsp;mg\/mL, respectively. Notably, both agents exhibited a strong dose-dependent inhibitory effect on biofilm formation. While Cs-TPA-PiP showed lower MIC values against planktonic cells, the corresponding Cs-TPA-PiP NPs with an ultra-small spherical size of 15.6&amp;nbsp;nm exhibited superior antibiofilm performance, ranging from 73.00% to 95.00% inhibition of biofilm biomass at 1&#215; MIC in strong biofilm-producing strains. Transmission electron microscopy (TEM) confirmed severe morphological alterations and membrane disruption in treated bacterial cells, consistent with a membrane-targeting mechanism. In silico molecular docking studies suggested that the compound has favorable binding affinity for the critical bacterial cell wall target, Sortase A, thereby identifying it as a potential theoretical target requiring further validation. Our findings collectively establish Cs-TPA-PiP and its Cs-TPA-PiP NPs as effective antibacterial and anti-biofilm candidates, with their activity primarily attributed to membrane disruption. The proposed role of Sortase A inhibition remains hypothetical and warrants further investigation. 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