[HTML][HTML] Emerging role of biopharmaceutical classification and biopharmaceutical drug disposition system in dosage form development: A systematic review

R Samineni, J Chimakurthy… - Turkish journal of …, 2022 - ncbi.nlm.nih.gov
Biopharmaceutical classification system (BCS) is an advanced tool used for classifying
medicines based on dissolution, water solubility, and intestinal permeability, which affect the …

[HTML][HTML] Comparison between the dissolution profiles of nine meloxicam tablet brands commercially available in Buenos Aires, Argentina

LD Simionato, L Petrone, M Baldut, SL Bonafede… - Saudi pharmaceutical …, 2018 - Elsevier
In this work, the dissolution profiles of nine meloxicam tablet brands marketed in Argentina
have been evaluated. As meloxicam is a Class 2 Biopharmaceutical Classification System …

[HTML][HTML] Development and characterization of an atorvastatin solid dispersion formulation using skimmed milk for improved oral bioavailability

A Choudhary, AC Rana, G Aggarwal, V Kumar… - … Pharmaceutica Sinica B, 2012 - Elsevier
Atorvastatin has low aqueous solubility resulting in low oral bioavailability (12%) and thus
presents a challenge in formulating a suitable dosage form. To improve the aqueous …

Study of top-down and bottom-up approaches by using design of experiment (DoE) to produce meloxicam nanocrystal capsules

T Liu, X Yu, H Yin - Aaps Pharmscitech, 2020 - Springer
In order to investigate the correlation among energy input–related, drug-related, and
stabilizer-related aspects for both top-down and bottom-up nanocrystal production …

Curcumin-loaded soluplus® based ternary solid dispersions with enhanced solubility, dissolution and antibacterial, antioxidant, anti-inflammatory activities

M Ishtiaq, H Manzoor, IU Khan, S Asghar, M Irfan… - Heliyon, 2024 - cell.com
Amorphous solid dispersion (ASD) has emerged to be an outstanding strategy among
multiple options available for improving solubility and consequently biological activity …

Study of the parameters influencing the co-grinding process for the production of meloxicam nanoparticles

L Kürti, Á Kukovecz, G Kozma, R Ambrus, MA Deli… - Powder technology, 2011 - Elsevier
Co-grinding is a procedure for the preparation of nanoparticles in which the drug is ground
together with one or more excipients. The grinding of meloxicam, a crystalline solid, together …

Natural polymer chitosan as super disintegrant in fast orally disintegrating meloxicam tablets: Formulation and evaluation

G Draksiene, B Venclovaite, L Pudziuvelyte… - Pharmaceutics, 2021 - mdpi.com
The aim of the present investigation was to formulate fast disintegrating tablets of meloxicam
by wet granulation technique using medium molecular weight chitosan. The orally …

Solubility and solution thermodynamics of meloxicam in polyethylene glycol 400+ water mixtures

ZJ Cárdenas, DM Jiménez, F Martínez - Journal of Molecular Liquids, 2015 - Elsevier
The equilibrium solubility of meloxicam (MEL) in polyethylene glycol (PEG) 400+ water
binary mixtures at temperatures from 298.15 K to 318.15 K was determined and the …

Preparation and characterization of cefuroxime axetil solid dispersions using poloxamer 188

T Sankari, S Al-Hariri - Brazilian Journal of Pharmaceutical Sciences, 2019 - SciELO Brasil
The main objective of the present work was to enhance the solubility and dissolution rate of
poorly water-soluble drug cefuroxime axetil (CA) by formulating it into solid dispersions …

Formulation and evaluation of liquisolid compacts of itraconazole to enhance its oral bioavailability

HP Thakkar, D Vasava, AA Patel… - Therapeutic Delivery, 2020 - Taylor & Francis
Aim: Formulate and evaluate liquisolid compacts of Itraconazole, a biopharmaceutical
classification system class II drug, which has poor bioavailability. Materials & methods: PEG …