Controlled drug delivery systems: current status and future directions

S Adepu, S Ramakrishna - Molecules, 2021 - mdpi.com
The drug delivery system enables the release of the active pharmaceutical ingredient to
achieve a desired therapeutic response. Conventional drug delivery systems (tablets …

Occurrence, removal and risk evaluation of ibuprofen and acetaminophen in municipal wastewater treatment plants: A critical review

Z Liu, Q Ma, L Dai, Z Dang - Science of the Total Environment, 2023 - Elsevier
Ibuprofen and acetaminophen as two anti-fever agents have been widely used in human.
Due to lack of full understanding, this work firstly summarized their occurrence and fate in …

Hydroxypropyl methylcellulose-based controlled release dosage by melt extrusion and 3D printing: Structure and drug release correlation

J Zhang, W Yang, AQ Vo, X Feng, X Ye, DW Kim… - Carbohydrate …, 2017 - Elsevier
The objective of this study was to develop a new approach for fabrication of zero order
release of active pharmaceutical ingredients (APIs) using hot-melt extrusion (HME) and 3D …

Prediction of solubility and permeability class membership: provisional BCS classification of the world's top oral drugs

A Dahan, JM Miller, GL Amidon - The AAPS journal, 2009 - Springer
Abstract The Biopharmaceutics Classification System (BCS) categorizes drugs into one of
four biopharmaceutical classes according to their water solubility and membrane …

[图书][B] Handbook of Pharmaceutical Manufacturing Formulations: Volume Two, Uncompressed Solid Products

SK Niazi - 2019 - taylorfrancis.com
The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Two,
Uncompressed Solid Products is an authoritative and practical guide to the art and science …

Biowaiver monographs for immediate release solid oral dosage forms: Diclofenac sodium and diclofenac potassium

B Chuasuwan, V Binjesoh, JE Polli, H Zhang… - Journal of …, 2009 - Elsevier
Literature data are reviewed regarding the scientific advisability of allowing a waiver of in
vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage …

Paracetamol extended release FDM 3D printlets: Evaluation of formulation variables on printability and drug release

M Đuranović, S Obeid, M Madžarević, S Cvijić… - International journal of …, 2021 - Elsevier
Paracetamol printlets were prepared via hot-melt extrusion process and fused deposition
modelling, using two types of backbone polymers. Polycaprolactone (PCL) and …

Biowaiver monographs for immediate release solid oral dosage forms: furosemide

GE Granero, MR Longhi, MJ Mora… - Journal of …, 2010 - Elsevier
Literature and new experimental data relevant to the decision to allow a waiver of in vivo
bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage …

Evolution of a detailed physiological model to simulate the gastrointestinal transit and absorption process in humans, part 1: oral solutions

K Thelen, K Coboeken, S Willmann, R Burghaus… - Journal of …, 2011 - Elsevier
To enable more precise prediction of oral drug absorption, an existing physiologically based
absorption model was revised. The revised model reflects detailed knowledge of human …

Solubility behavior and biopharmaceutical classification of novel high-solubility ciprofloxacin and norfloxacin pharmaceutical derivatives

SA Breda, AF Jimenez-Kairuz, RH Manzo… - International journal of …, 2009 - Elsevier
The hydrochlorides of the 1: 3 aluminum: norfloxacin and aluminum: ciprofloxacin
complexes were characterized according to the Biopharmaceutics Classification System …