Liquid and solid self-emulsifying drug delivery systems (SEDDs) as carriers for the oral delivery of azithromycin: optimization, in vitro characterization and stability …

R Abou Assi, I M. Abdulbaqi, T Seok Ming, C Siok Yee… - Pharmaceutics, 2020 - mdpi.com
Azithromycin (AZM) is a macrolide antibiotic used for the treatment of various bacterial
infections. The drug is known to have low oral bioavailability (37%) which may be attributed …

Antimicrobial and immunomodulatory surface‐functionalized electrospun membranes for bone regeneration

A Mathew, C Vaquette, S Hashimi… - Advanced …, 2017 - Wiley Online Library
Guided bone regeneration (GBR) is a surgical procedure utilizing occlusive membranes for
providing space maintenance and enabling selective repopulation of the damaged area …

Degradation of high concentrations of azithromycin when present in a high organic content wastewater by using a continuously fed laboratory-scale UASB bioreactor

MP Martínez-Polanco, JA Valderrama-Rincón… - Chemosphere, 2022 - Elsevier
As the presence of emergent contaminants in wastewater, such as antibiotics, has become a
threat for public health, the evaluation of strategies to treat them has been gaining …

[HTML][HTML] Formulation of Thermo-Sensitive In Situ Gels Loaded with Dual Spectrum Antibiotics of Azithromycin and Ofloxacin

R Alsheikh, Á Haimhoffer, D Nemes, Z Ujhelyi, P Fehér… - Polymers, 2024 - mdpi.com
In situ gels have been developed as an innovative strategy to prolong corneal residence
time and enhance drug absorption compared to traditional eye drops. Our study aimed to …

Amorphous azithromycin with improved aqueous solubility and intestinal membrane permeability

M Aucamp, R Odendaal, W Liebenberg… - Drug development and …, 2015 - Taylor & Francis
Azithromycin (AZM) is a poorly soluble macrolide antibacterial agent. Its low solubility is
considered as the major contributing factor to its relatively low oral bioavailability. The aim of …

Enhancing dissolution rate and antibacterial efficiency of azithromycin through drug-drug cocrystals with paracetamol

N Ul Islam, E Khan, M Naveed Umar, A Shah… - Antibiotics, 2021 - mdpi.com
Cocrystallization is a promising approach to alter physicochemical properties of active
pharmaceutical ingredients (hereafter abbreviated as APIs) bearing poor profile. Nowadays …

Influence of process and formulation parameters on dissolution and stability characteristics of Kollidon® VA 64 hot-melt extrudates

S Maddineni, SK Battu, J Morott, S Majumdar… - AAPS …, 2015 - Springer
The objective of the present study was to investigate the effects of processing variables and
formulation factors on the characteristics of hot-melt extrudates containing a copolymer …

Stabilized amorphous solid dispersions with small molecule excipients

K Löbmann, KT Jensen, R Laitinen, T Rades… - … Dispersions: Theory and …, 2014 - Springer
The application of small molecular weight compounds may be a way to overcome some of
the drawbacks of polymer-based amorphous solid dispersions, such as drug—polymer …

A review on delivery and bioavailability enhancement strategies of azithromycin

P Swarup, GP Agrawal - ASSAY and Drug Development …, 2022 - liebertpub.com
Azithromycin (AZI) belongs to the class of macrolide antibiotics that has limited water
solubility and belongs to Biopharmaceutical Classification System Class II. Dissolution is the …

[HTML][HTML] In vitro dissolution study of atorvastatin binary solid dispersion

R Jahan, MS Islam, A Tanwir… - Journal of Advanced …, 2013 - journals.lww.com
The aim of the present study was to improve the solubility and dissolution rate of atorvastatin
(ATV), a slight water-soluble drug, by solid dispersion (SD) technique using a hydrophilic …