Octa-Arginine-Conjugated Liposomal Nimodipine Incorporated in a Temperature-Responsive Gel for Nasoencephalic Delivery DOI

Shuai Hong,

Changxiu Lin,

Junsheng Hu

и другие.

Molecular Pharmaceutics, Год журнала: 2024, Номер 21(10), С. 5217 - 5237

Опубликована: Авг. 26, 2024

Nimodipine is the primary clinical drug used to treat cerebral vasospasm following subarachnoid hemorrhage. Currently, tablets have low bioavailability when taken orally, and injections contain ethanol. Therefore, we investigated a new method of nimodipine administration, namely, nasoencephalic administration. Nasal administration was carried out by attaching cell-penetrating peptide octa-arginine (R8) liposomes incorporating it into temperature-sensitive in situ gel. The prepared gels underwent separate evaluations for vitro characterization. In release exhibited significant slow-release effect. toad maxillary cilia model, RPMI 2650 cytotoxicity, vivo SD rat pathological histotoxicity experiments showed that all dosage from groups had no toxicity cilia, cells, tissues organs, continued oscillate up 694 ± 10.15 min, with survival rate cells being above 85%. A transwell nasal mucosa cell model an isolated porcine were established, results osmolality R8-modified liposomal gel mucosal 30.41 2.14 65.9 7.34 μg/mL, respectively, which significantly higher than NM-Solution PEGylated liposome groups. Animal fluorescence imaging studies revealed displayed increased brain intensity compared normal Pharmacokinetic after transnasal AUC

Язык: Английский

Fully biodegradable hierarchically designed high-performance nanocellulose piezo-arrays DOI Creative Commons
Sujoy Kumar Ghosh,

Francesca Matino,

Fabio Lineu Favrin

и другие.

Science Advances, Год журнала: 2025, Номер 11(3)

Опубликована: Янв. 15, 2025

While piezoelectric sensing and energy-harvesting devices still largely rely on inorganic components, biocompatible biodegradable materials, such as cellulose nanocrystals, might constitute optimal sustainable building blocks for a variety of applications in electronics transient implants. To this aim, however, effective methods are needed to position nanocrystals large high-performance architectures. Here, we report scalable assemblies multilayered systems with exceptional response, various application scopes. The submicrometer patterning effective-flow topography multilayer stacking promote performance. Record output power pressure sensitivity the gentle touch range obtained flexible, fully stable properties demonstrated compatibility different cell lines implanted devices. These architectures offer new design principles materials realizing an innovative class practical components mechanical energy harvesting biologically relevant wearables

Язык: Английский

Процитировано

4

Modeling and characterization of lenalidomide-loaded tripolyphosphate-crosslinked chitosan nanoparticles for anticancer drug delivery DOI

Afsaneh Moghaddam Jafari,

Ali Morsali, Mohammad Reza Bozorgmehr

и другие.

International Journal of Biological Macromolecules, Год журнала: 2024, Номер 260, С. 129360 - 129360

Опубликована: Янв. 11, 2024

Язык: Английский

Процитировано

10

Chitosan Nanoparticles for Intranasal Drug Delivery DOI Creative Commons
Hossein Omidian, Erma J. Gill, Sumana Dey Chowdhury

и другие.

Pharmaceutics, Год журнала: 2024, Номер 16(6), С. 746 - 746

Опубликована: Май 31, 2024

This manuscript explores the use of nanostructured chitosan for intranasal drug delivery, targeting improved therapeutic outcomes in neurodegenerative diseases, psychiatric care, pain management, vaccination, and diabetes treatment. Chitosan nanoparticles are shown to enhance brain improve bioavailability, minimize systemic side effects by facilitating transport across blood–brain barrier. Despite substantial advancements targeted delivery vaccine efficacy, challenges remain scalability, regulatory approval, transitioning from preclinical studies clinical applications. The future chitosan-based nanomedicines hinges on advancing trials, fostering interdisciplinary collaboration, innovating nanoparticle design overcome these hurdles realize their potential.

Язык: Английский

Процитировано

10

Chitosan nanoparticles for nasal drug delivery DOI Creative Commons

Salah Alghareeb,

Ifeoma Cynthia Ekenna, Kofi Asare‐Addo

и другие.

Journal of Drug Delivery Science and Technology, Год журнала: 2025, Номер unknown, С. 106623 - 106623

Опубликована: Янв. 1, 2025

Процитировано

1

Development of nanomedicines for the treatment of Alzheimer’s disease: Raison d’être, strategies, challenges and regulatory aspects DOI
Farhan Mazahir,

Md Imtiyaz Alam,

Awesh K. Yadav

и другие.

Ageing Research Reviews, Год журнала: 2024, Номер 98, С. 102318 - 102318

Опубликована: Май 4, 2024

Язык: Английский

Процитировано

3

Chitosan: Structural and Chemical Modification, Properties, and Application DOI Open Access
Joanna Kluczka

International Journal of Molecular Sciences, Год журнала: 2023, Номер 25(1), С. 554 - 554

Опубликована: Дек. 31, 2023

Chitosan is a polymer of natural origins that possesses many favourable properties [...]

Язык: Английский

Процитировано

5

Polyphenol-Enabled 2D Nanopatch for Enhanced Nasal Mucoadhesion and Immune Activation DOI
Jeong Pil Han,

Yu Ri Nam,

Hye Yoon Chung

и другие.

Nano Letters, Год журнала: 2024, Номер 24(33), С. 10380 - 10387

Опубликована: Авг. 9, 2024

The advancement of effective nasal mucoadhesive delivery faces challenges due to rapid mucociliary clearance (MCC). Conventional studies have employed materials, mainly forming spherical nanoparticles, but these offer limited adhesion the mucosa. This study hypothesizes that a 2D nanoscale structure utilizing adhesive polyphenols can provide superior strategy for countering MCC, aligning with planar mucosal layers. We explore use tannic acid (TA), polyphenolic molecule known its properties and ability form complexes biomolecules. Our introduces an unprecedented nanopatch, assembled through interaction TA green fluorescent protein (GFP), cell-penetrating peptide (CPP). nanopatch demonstrates robust mucosa significantly enhances immunoglobulin A secretions, suggesting potential enhancing vaccine delivery. promise polyphenol-enabled signifies pivotal shift from conventional opening new pathways strategies respiratory mucoadhesion.

Язык: Английский

Процитировано

1

Bile acid conjugated chitosan nanoparticles promote the proliferation and epithelial-mesenchymal transition of hepatocellular carcinoma by regulating the PI3K/Akt/mTOR pathway DOI
Ziyu Jiang, Yi Xu,

Liu Yang

и другие.

Carbohydrate Research, Год журнала: 2024, Номер 545, С. 109296 - 109296

Опубликована: Окт. 23, 2024

Язык: Английский

Процитировано

1

Octa-Arginine-Conjugated Liposomal Nimodipine Incorporated in a Temperature-Responsive Gel for Nasoencephalic Delivery DOI

Shuai Hong,

Changxiu Lin,

Junsheng Hu

и другие.

Molecular Pharmaceutics, Год журнала: 2024, Номер 21(10), С. 5217 - 5237

Опубликована: Авг. 26, 2024

Nimodipine is the primary clinical drug used to treat cerebral vasospasm following subarachnoid hemorrhage. Currently, tablets have low bioavailability when taken orally, and injections contain ethanol. Therefore, we investigated a new method of nimodipine administration, namely, nasoencephalic administration. Nasal administration was carried out by attaching cell-penetrating peptide octa-arginine (R8) liposomes incorporating it into temperature-sensitive in situ gel. The prepared gels underwent separate evaluations for vitro characterization. In release exhibited significant slow-release effect. toad maxillary cilia model, RPMI 2650 cytotoxicity, vivo SD rat pathological histotoxicity experiments showed that all dosage from groups had no toxicity cilia, cells, tissues organs, continued oscillate up 694 ± 10.15 min, with survival rate cells being above 85%. A transwell nasal mucosa cell model an isolated porcine were established, results osmolality R8-modified liposomal gel mucosal 30.41 2.14 65.9 7.34 μg/mL, respectively, which significantly higher than NM-Solution PEGylated liposome groups. Animal fluorescence imaging studies revealed displayed increased brain intensity compared normal Pharmacokinetic after transnasal AUC

Язык: Английский

Процитировано

0