Amino acids as the potential co-former for co-crystal development: a review
I Nugrahani, MA Jessica - Molecules, 2021 - mdpi.com
Co-crystals are one of the most popular ways to modify the physicochemical properties of
active pharmaceutical ingredients (API) without changing pharmacological activity through …
active pharmaceutical ingredients (API) without changing pharmacological activity through …
Nano spray-dried drugs for oral administration: A review
AA Öztürk, C Arpagaus - ASSAY and Drug Development …, 2021 - liebertpub.com
Spray drying is an important technology that is fast, simple, reproducible, and scalable. It has
a wide application range, that is, in food, chemicals, and encapsulation of pharmaceuticals …
a wide application range, that is, in food, chemicals, and encapsulation of pharmaceuticals …
[HTML][HTML] A comparison study of lipid and polymeric nanoparticles in the nasal delivery of meloxicam: Formulation, characterization, and in vitro evaluation
With the increasingly widespread of central nervous system (CNS) disorders and the lack of
sufficiently effective medication, meloxicam (MEL) has been reported as a possible …
sufficiently effective medication, meloxicam (MEL) has been reported as a possible …
Spray-freeze-dried inhalable composite microparticles containing nanoparticles of combinational drugs for potential treatment of lung infections caused by …
The multi-drug resistance of Pseudomonas aeruginosa is an overwhelming cause of
terminal and persistent lung infections in cystic fibrosis (CF) patients. Antimicrobial synergy …
terminal and persistent lung infections in cystic fibrosis (CF) patients. Antimicrobial synergy …
Development and evaluation of TPGS/PVA-based nanosuspension for enhancing dissolution and oral bioavailability of ticagrelor
In this study, we developed ticagrelor-dispersed nanosuspension (TCG-NSP) to enhance
the dissolution and oral bioavailability of ticagrelor (TCG) through a statistical design …
the dissolution and oral bioavailability of ticagrelor (TCG) through a statistical design …
Preparation and characterization of soluplus-based nanosuspension for dissolution enhancement of indomethacin using ultrasonic assisted precipitation method for …
Objectives Nanosuspensions are increasingly recognized as a valuable technology for
enhancing poorly water-soluble drugs' solubility and dissolution rate, thereby improving their …
enhancing poorly water-soluble drugs' solubility and dissolution rate, thereby improving their …
Tannic acid coated nanosuspension for oral delivery of chrysin intended for anti-schizophrenic effect in mice
Chrysin is a flavonoid drug with numerous therapeutic activities. It suffers from low intestinal
absorption owing to its hydrophobicity. Therefore, the aim of this study is to exploit the …
absorption owing to its hydrophobicity. Therefore, the aim of this study is to exploit the …
RETRACTED ARTICLE: Formulation of Aceclofenac Tablets Using Nanosuspension as Granulating Agent: An Attempt to Enhance Dissolution Rate and Oral …
H Rahim, A Sadiq, R Ullah, A Bari, F Amin… - International Journal …, 2020 - Taylor & Francis
Rahim H, Sadiq A, Ullah R, et al. Int J Nanomedicine. 2020; 15: 8999–9009. We, the Editors
and Publisher of International Journal of Nanomedicine, have retracted the following article …
and Publisher of International Journal of Nanomedicine, have retracted the following article …
[HTML][HTML] Ultrasensitive and simultaneous detection of 6 nonsteroidal anti-inflammatory drugs by colloidal gold strip sensor
In this work, an oxicam group–selective monoclonal antibody against 6 nonsteroidal anti-
inflammatory drugs (NSAID; meloxicam, lornoxicam, piroxicam, sudoxicam, droxicam, and …
inflammatory drugs (NSAID; meloxicam, lornoxicam, piroxicam, sudoxicam, droxicam, and …
Development of Dermal Lidocaine Nanosuspension Formulation by the Wet Milling Method Using Experimental Design: In Vitro/In Vivo Evaluation
O Kral, S Ilbasmis-Tamer, S Han, F Tirnaksiz - ACS omega, 2024 - ACS Publications
Lidocaine (LID), frequently used in dermal applications, is a nonpolar local anesthetic agent
that is practically insoluble in water. The main aim of this study is to develop the …
that is practically insoluble in water. The main aim of this study is to develop the …