{"title":"Curcumin-loaded PEG-functionalized carbon nanotubes: a novel strategy for Alzheimer's management.","authors":"Shrutee Pawar, Vasanti Suvarna","doi":"10.1080/20415990.2025.2513213","DOIUrl":null,"url":null,"abstract":"<p><strong>Aims: </strong>Curcumin (CUR) exhibits strong therapeutic potential for Alzheimer's disease due to its antioxidant, neuroprotective, anti-inflammatory, and anti-amyloid effects. However, its clinical application is limited by poor brain bioavailability. This study aimed to enhance CUR delivery to the brain via nasal administration using a novel formulation of polyethylene glycol (PEG)-functionalized carboxylated (COOH) Multi-Walled Carbon Nanotubes (MWCNT).</p><p><strong>Materials and methods: </strong>CUR-loaded MWCNT-COOH-PEG was developed and optimized using a 3<sup>2</sup> factorial design. The system was characterized for entrapment efficiency, particle size, zeta potential, and in vitro release. Neuroprotective efficacy was assessed through apoptosis inhibition in PC12 cells, and CUR concentration in the brain was measured post-nasal administration.</p><p><strong>Results: </strong>The formulation achieved an entrapment efficiency of 91.4 ± 0.8%, a zeta potential of -31.1 ± 1.05 mV, and a particle size of 310 ± 7.92 nm. In vitro release was 95.42 ± 0.0004% at pH 5.5 and 89.98 ± 0.0039% at pH 7.4. CUR at 18.75 µg/mL inhibited apoptosis in PC12 cells after 24 h. Higher brain CUR concentrations were observed 4 h post-administration.</p><p><strong>Conclusion: </strong>CUR-loaded MWCNT-COOH-PEG effectively enhances brain bioavailability of CUR, demonstrating significant neuroprotective effects, and offers a promising approach for Alzheimer's therapy.</p>","PeriodicalId":22959,"journal":{"name":"Therapeutic delivery","volume":" ","pages":"1-9"},"PeriodicalIF":3.0000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutic delivery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/20415990.2025.2513213","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Aims: Curcumin (CUR) exhibits strong therapeutic potential for Alzheimer's disease due to its antioxidant, neuroprotective, anti-inflammatory, and anti-amyloid effects. However, its clinical application is limited by poor brain bioavailability. This study aimed to enhance CUR delivery to the brain via nasal administration using a novel formulation of polyethylene glycol (PEG)-functionalized carboxylated (COOH) Multi-Walled Carbon Nanotubes (MWCNT).
Materials and methods: CUR-loaded MWCNT-COOH-PEG was developed and optimized using a 32 factorial design. The system was characterized for entrapment efficiency, particle size, zeta potential, and in vitro release. Neuroprotective efficacy was assessed through apoptosis inhibition in PC12 cells, and CUR concentration in the brain was measured post-nasal administration.
Results: The formulation achieved an entrapment efficiency of 91.4 ± 0.8%, a zeta potential of -31.1 ± 1.05 mV, and a particle size of 310 ± 7.92 nm. In vitro release was 95.42 ± 0.0004% at pH 5.5 and 89.98 ± 0.0039% at pH 7.4. CUR at 18.75 µg/mL inhibited apoptosis in PC12 cells after 24 h. Higher brain CUR concentrations were observed 4 h post-administration.
Conclusion: CUR-loaded MWCNT-COOH-PEG effectively enhances brain bioavailability of CUR, demonstrating significant neuroprotective effects, and offers a promising approach for Alzheimer's therapy.
期刊介绍:
Delivering therapeutics in a way that is right for the patient - safe, painless, reliable, targeted, efficient and cost effective - is the fundamental aim of scientists working in this area. Correspondingly, this evolving field has already yielded a diversity of delivery methods, including injectors, controlled release formulations, drug eluting implants and transdermal patches. Rapid technological advances and the desire to improve the efficacy and safety profile of existing medications by specific targeting to the site of action, combined with the drive to improve patient compliance, continue to fuel rapid research progress. Furthermore, the emergence of cell-based therapeutics and biopharmaceuticals such as proteins, peptides and nucleotides presents scientists with new and exciting challenges for the application of therapeutic delivery science and technology. Successful delivery strategies increasingly rely upon collaboration across a diversity of fields, including biology, chemistry, pharmacology, nanotechnology, physiology, materials science and engineering. Therapeutic Delivery recognizes the importance of this diverse research platform and encourages the publication of articles that reflect the highly interdisciplinary nature of the field. In a highly competitive industry, Therapeutic Delivery provides the busy researcher with a forum for the rapid publication of original research and critical reviews of all the latest relevant and significant developments, and focuses on how the technological, pharmacological, clinical and physiological aspects come together to successfully deliver modern therapeutics to patients. The journal delivers this essential information in concise, at-a-glance article formats that are readily accessible to the full spectrum of therapeutic delivery researchers.