{"title":"芦荟提取物负载壳聚糖纳米颗粒的制备及其在四氯化碳肝损伤大鼠模型中的控制传递","authors":"Omar Ashraf, Alyaa Farid, Gehan Safwat","doi":"10.1186/s43088-025-00663-5","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>A significant contributing factor to liver damage is drug consumption. Phytochemicals of <i>Aloe vera</i> extract are effective against a variety of diseases. Consequently, this study aimed to create chitosan nanoparticles (chi NPs) that were loaded with <i>Aloe vera</i> extract (ALV extract) to increase the delivery of the extract's bioactive materials. ALV extract, chi NPs, and <i>Aloe vera</i> extract-loaded chitosan nanoparticles (ALV-chi NPs) underwent anti-oxidant, anti-inflammatory, and cytotoxicity tests. The preventive and therapeutic effects of ALV-chi NPs against carbon tetrachloride (CCl4)-induced liver injury were assessed using a male Sprague Dawley rat model.</p><h3>Results</h3><p>Our findings demonstrated that the synthesis of ALV-chi NPs was a promising option for combining the therapeutic benefits of both ALV extract (included in its phytochemicals) and chi NPs. ALV-chi NPs have a uniformly distributed smooth shape with a size of 48.3 ± 2.97 nm, similar to the hydrodynamic size (50.9 ± 0.07 nm), and a surface charge of 38.16 mV. At a 1000 μg/mL concentration, ALV-chi NPs showed high DPPH scavenging % and a high hemolysis inhibition %. At 75 μg/mL, ALV-chi NPs showed lower PTT (63.7 s) than ALV extract (71.2 s). The phenolic components and flavonoids in the extract were released under controlled conditions throughout time, and their bioavailability was enhanced by loading the extract on chi NPs.</p><h3>Conclusions</h3><p>Among all tested formulations, ALV-chi NPs demonstrated superior efficacy, showing 95.4% DPPH scavenging (vs. 91.8% for free extract), 94.1% hemolysis inhibition (comparable to indomethacin), and optimal hepatoprotection in CCl4-induced liver injury. ALV-chi NPs ameliorated the raised levels of liver function parameters, pro-inflammatory cytokines, and intracellular apoptotic proteins.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":481,"journal":{"name":"Beni-Suef University Journal of Basic and Applied Sciences","volume":"14 1","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://bjbas.springeropen.com/counter/pdf/10.1186/s43088-025-00663-5","citationCount":"0","resultStr":"{\"title\":\"Preparation of Aloe vera extract-loaded chitosan nanoparticles for the controlled delivery of extract phytochemicals in carbon tetrachloride-induced liver injury rat model\",\"authors\":\"Omar Ashraf, Alyaa Farid, Gehan Safwat\",\"doi\":\"10.1186/s43088-025-00663-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>A significant contributing factor to liver damage is drug consumption. Phytochemicals of <i>Aloe vera</i> extract are effective against a variety of diseases. Consequently, this study aimed to create chitosan nanoparticles (chi NPs) that were loaded with <i>Aloe vera</i> extract (ALV extract) to increase the delivery of the extract's bioactive materials. ALV extract, chi NPs, and <i>Aloe vera</i> extract-loaded chitosan nanoparticles (ALV-chi NPs) underwent anti-oxidant, anti-inflammatory, and cytotoxicity tests. The preventive and therapeutic effects of ALV-chi NPs against carbon tetrachloride (CCl4)-induced liver injury were assessed using a male Sprague Dawley rat model.</p><h3>Results</h3><p>Our findings demonstrated that the synthesis of ALV-chi NPs was a promising option for combining the therapeutic benefits of both ALV extract (included in its phytochemicals) and chi NPs. ALV-chi NPs have a uniformly distributed smooth shape with a size of 48.3 ± 2.97 nm, similar to the hydrodynamic size (50.9 ± 0.07 nm), and a surface charge of 38.16 mV. At a 1000 μg/mL concentration, ALV-chi NPs showed high DPPH scavenging % and a high hemolysis inhibition %. At 75 μg/mL, ALV-chi NPs showed lower PTT (63.7 s) than ALV extract (71.2 s). The phenolic components and flavonoids in the extract were released under controlled conditions throughout time, and their bioavailability was enhanced by loading the extract on chi NPs.</p><h3>Conclusions</h3><p>Among all tested formulations, ALV-chi NPs demonstrated superior efficacy, showing 95.4% DPPH scavenging (vs. 91.8% for free extract), 94.1% hemolysis inhibition (comparable to indomethacin), and optimal hepatoprotection in CCl4-induced liver injury. ALV-chi NPs ameliorated the raised levels of liver function parameters, pro-inflammatory cytokines, and intracellular apoptotic proteins.</p><h3>Graphical abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":481,\"journal\":{\"name\":\"Beni-Suef University Journal of Basic and Applied Sciences\",\"volume\":\"14 1\",\"pages\":\"\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://bjbas.springeropen.com/counter/pdf/10.1186/s43088-025-00663-5\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Beni-Suef University Journal of Basic and Applied Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.1186/s43088-025-00663-5\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Beni-Suef University Journal of Basic and Applied Sciences","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1186/s43088-025-00663-5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Preparation of Aloe vera extract-loaded chitosan nanoparticles for the controlled delivery of extract phytochemicals in carbon tetrachloride-induced liver injury rat model
Background
A significant contributing factor to liver damage is drug consumption. Phytochemicals of Aloe vera extract are effective against a variety of diseases. Consequently, this study aimed to create chitosan nanoparticles (chi NPs) that were loaded with Aloe vera extract (ALV extract) to increase the delivery of the extract's bioactive materials. ALV extract, chi NPs, and Aloe vera extract-loaded chitosan nanoparticles (ALV-chi NPs) underwent anti-oxidant, anti-inflammatory, and cytotoxicity tests. The preventive and therapeutic effects of ALV-chi NPs against carbon tetrachloride (CCl4)-induced liver injury were assessed using a male Sprague Dawley rat model.
Results
Our findings demonstrated that the synthesis of ALV-chi NPs was a promising option for combining the therapeutic benefits of both ALV extract (included in its phytochemicals) and chi NPs. ALV-chi NPs have a uniformly distributed smooth shape with a size of 48.3 ± 2.97 nm, similar to the hydrodynamic size (50.9 ± 0.07 nm), and a surface charge of 38.16 mV. At a 1000 μg/mL concentration, ALV-chi NPs showed high DPPH scavenging % and a high hemolysis inhibition %. At 75 μg/mL, ALV-chi NPs showed lower PTT (63.7 s) than ALV extract (71.2 s). The phenolic components and flavonoids in the extract were released under controlled conditions throughout time, and their bioavailability was enhanced by loading the extract on chi NPs.
Conclusions
Among all tested formulations, ALV-chi NPs demonstrated superior efficacy, showing 95.4% DPPH scavenging (vs. 91.8% for free extract), 94.1% hemolysis inhibition (comparable to indomethacin), and optimal hepatoprotection in CCl4-induced liver injury. ALV-chi NPs ameliorated the raised levels of liver function parameters, pro-inflammatory cytokines, and intracellular apoptotic proteins.
期刊介绍：
Beni-Suef University Journal of Basic and Applied Sciences (BJBAS) is a peer-reviewed, open-access journal. This journal welcomes submissions of original research, literature reviews, and editorials in its respected fields of fundamental science, applied science (with a particular focus on the fields of applied nanotechnology and biotechnology), medical sciences, pharmaceutical sciences, and engineering. The multidisciplinary aspects of the journal encourage global collaboration between researchers in multiple fields and provide cross-disciplinary dissemination of findings.
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