Nanomedicine for the effective and safe delivery of non-steroidal anti-inflammatory drugs: A review of preclinical research

H Al-Lawati, Z Binkhathlan, A Lavasanifar - European Journal of …, 2019 - Elsevier
The toxicity of nonsteroidal anti-inflammatory drugs (NSAIDs) is one of the major limitations
to their long-term use in the treatment of chronic inflammatory conditions. This review …

A hyaluronic acid functionalized self-nano-emulsifying drug delivery system (SNEDDS) for enhancement in ciprofloxacin targeted delivery against intracellular …

R Arshad, TA Tabish, MH Kiani, IM Ibrahim, G Shahnaz… - Nanomaterials, 2021 - mdpi.com
Ciprofloxacin (CIP), a potent anti-bacterial agent of the fluroquinolone family, shows poor
solubility and permeability, thus leading to the development of intracellular pathogens …

[HTML][HTML] Attenuation of celecoxib cardiac toxicity using Poly (δ-decalactone) based nanoemulsion via oral route

S Maru, J Verma, CE Wilen, JM Rosenholm… - European Journal of …, 2023 - Elsevier
Celecoxib (CLX), a poorly soluble anti-inflammatory drug, requires administration in higher
concentrations to produce therapeutic effects, oftentimes resulting in cardiac toxicity …

Improving the efficacy of Cyclooxegenase-2 inhibitors in the management of oral cancer: Insights into the implementation of nanotechnology and mucoadhesion

AA Mabrouk, MI Tadros, WM El-Refaie - Journal of Drug Delivery Science …, 2021 - Elsevier
Oral carcinoma is a worldwide health threat with high rate of recurrence and metastasis.
Cyclooxygenase-2 (COX-2) enzyme is over expressed in oral cancer cells and affects …

Oral gel loaded with penciclovir–lavender oil nanoemulsion to enhance bioavailability and alleviate pain associated with herpes labialis

KM Hosny, AM Sindi, HM Alkhalidi, M Kurakula… - Drug Delivery, 2021 - Taylor & Francis
Herpes labialis, caused by herpes simplex virus type 1, is usually characterized by painful
skin or mucosal lesions. Penciclovir (PV) tablets are found to be effective against herpes …

Mechanistic studies on the absorption enhancement of a self-nanoemulsifying drug delivery system loaded with norisoboldine-phospholipid complex

J Zhang, X Wen, Y Dai, Y Xia - International journal of …, 2019 - Taylor & Francis
Background Norisoboldine (NOR), the main isoquinoline alkaloid constituent in Radix
Linderae, was demonstrated to have an outstanding anti-arthritis activity. However, a poor …

Comparison of two self-nanoemulsifying drug delivery systems using different solidification techniques for enhanced solubility and oral bioavailability of poorly water …

MR Woo, S Woo, YW Bak, S Cheon, JS Kim… - Colloids and Surfaces B …, 2024 - Elsevier
In this study, we aimed to develop a solid self-nanoemulsifying drug delivery system (S-
SNEDDS) and a solid self-nanoemulsifying granule system (S-SNEGS) to enhance the …

A customized screening tool approach for the development of a self-nanoemulsifying drug delivery system (SNEDDS)

FP Schmied, A Bernhardt, A Engel, S Klein - AAPS PharmSciTech, 2021 - Springer
The present study focused on establishing a novel,(pre-) screening approach that enables
the development of promising performing self-nanoemulsifying drug delivery systems …

Buccal mucosal accumulation of dapoxetine using supersaturation, co-solvent and permeation enhancing polymer strategy

MA Akl, MA Hady, OM Sayed - Journal of Drug Delivery Science and …, 2020 - Elsevier
Purpose we have presented the potential of using mixed solvents, supersaturation and
penetration enhancing polymers for achieving a good route for poorly soluble and …

Spray-dried self-nanoemulsifying drug delivery systems as carriers for the oral delivery of piperine: Characterization and in vitro evaluation

N Kusumorini, AK Nugroho, S Pramono… - Journal of Applied …, 2022 - japsonline.com
Piperine is the primary alkaloid compound of white pepper, which has many therapeutic
benefits. However, piperine has limitations, including low bioavailability, being …