Lipid-based nanovesicular drug delivery systems

T Limongi, F Susa, M Marini, M Allione, B Torre… - Nanomaterials, 2021 - mdpi.com
In designing a new drug, considering the preferred route of administration, various
requirements must be fulfilled. Active molecules pharmacokinetics should be reliable with a …

[HTML][HTML] Niosome as a promising tool for increasing the effectiveness of anti-inflammatory compounds

MS Fadaei, MR Fadaei, AE Kheirieh… - EXCLI …, 2024 - ncbi.nlm.nih.gov
Niosomes are drug delivery systems with widespread applications in pharmaceutical
research and the cosmetic industry. Niosomes are vesicles of one or more bilayers made of …

Optimization and characterization of tannic acid loaded niosomes for enhanced antibacterial and anti-biofilm activities

F Heidari, I Akbarzadeh, D Nourouzian… - Advanced Powder …, 2020 - Elsevier
The purpose of this study was to prepare and characterize an optimized system of tannic
acid-loaded niosomes as a potential carrier for antibacterial and anti-biofilm delivery. The …

Development of provesicular nanodelivery system of curcumin as a safe and effective antiviral agent: statistical optimization, in vitro characterization, and antiviral …

FA Badria, AE Abdelaziz, AH Hassan, AA Elgazar… - Molecules, 2020 - mdpi.com
Curcumin is a natural compound that has many medical applications. However, its low
solubility and poor stability could impede its clinical applications. The present study aimed to …

Construction and characterization of a novel Tenofovir-loaded PEGylated niosome conjugated with TAT peptide for evaluation of its cytotoxicity and anti-HIV effects

MS Yadavar-Nikravesh, S Ahmadi, A Milani… - Advanced Powder …, 2021 - Elsevier
In recent years, nanocarriers have become potent drug delivery system candidates,
especially in anti-HIV therapies. Meanwhile, using cell-penetrating peptides such as TAT for …

PEGylated Lipid Polymeric Nanoparticle–Encapsulated Acyclovir for In Vitro Controlled Release and Ex Vivo Gut Sac Permeation

S Mahmood, KC Kiong, CS Tham, TC Chien… - Aaps Pharmscitech, 2020 - Springer
Currently, pharmaceutical research is directed wide range for developing new drugs for oral
administration to target disease. Acyclovir formulation is having common issues of short half …

Oral proniosomal amitriptyline and liraglutide for management of diabetic neuropathy: Exceptional control over hyperglycemia and neuropathic pain

RG Eissa, NG Eissa, RA Eissa, NH Diab… - International Journal of …, 2023 - Elsevier
Exploitation of nanocarriers provides a compartment for enclosing drugs to protect them from
degradation and potentiate their therapeutic efficiency. In the current study, amitriptyline-and …

Proniosomal gel for topical delivery of rutin: Preparation, physicochemical characterization and in vitro toxicological profile using 3D reconstructed human epidermis …

I Pinzaru, A Tanase, V Enatescu, D Coricovac… - Antioxidants, 2021 - mdpi.com
Rutin (Rut) is a natural flavonol, well-known for its broad-spectrum of therapeutic effects,
including antioxidant and antitumoral activities; still, it has a reduced clinical outcome due to …

[HTML][HTML] Formulation of Glibenclamide proniosomes for oral administration: Pharmaceutical and pharmacodynamics evaluation

D Alshora, M Ibrahim, N Alanazi, M Alowyid… - Saudi Pharmaceutical …, 2023 - Elsevier
Glibenclamide (GB), oral antidiabetic sulfonylurea, is used in the management of diabetes
mellitus type II. It suffers from low bioavailability due to low water solubility. This work aimed …

Design and development of a proniosomal transdermal drug delivery system of caffeine for management of migraine: In vitro characterization, 131I-radiolabeling and …

MH Aboumanei, AF Mahmoud - Process Biochemistry, 2020 - Elsevier
Caffeine is a naturally occurring alkaloid compound which is widely used alone or in
combination in the treatment of migraine. The short elimination half life of caffeine (3− 5 h) …