Natural biomaterials for cardiac tissue engineering: a highly biocompatible solution

QA Majid, ATR Fricker, DA Gregory… - Frontiers in …, 2020 - frontiersin.org
Cardiovascular diseases (CVD) constitute a major fraction of the current major global
diseases and lead to about 30% of the deaths, ie, 17.9 million deaths per year. CVD include …

Eutectic mixtures as an approach to enhance solubility, dissolution rate and oral bioavailability of poorly water-soluble drugs

GC Bazzo, BR Pezzini, HK Stulzer - International Journal of Pharmaceutics, 2020 - Elsevier
Eutectic mixtures have been known for a long time in the pharmaceutical field. However, its
potential as a system to improve the solubility and dissolution of poorly water-soluble drugs …

Soluplus-mediated diosgenin amorphous solid dispersion with high solubility and high stability: development, characterization and oral bioavailability

P Liu, J Zhou, J Chang, X Liu, H Xue… - Drug design …, 2020 - Taylor & Francis
Background and Purpose The traditional Chinese medicine, diosgenin (Dio), has attracted
increasing attention because it possesses various therapeutic effects, including anti-tumor …

Cellulose derivatives as effective recrystallization inhibitor for ternary ritonavir solid dispersions: In vitro-in vivo evaluation

Q Guan, Q Ma, Y Zhao, X Jiang, H Zhang, M Liu… - Carbohydrate …, 2021 - Elsevier
Amorphous solid dispersions (ASDs) are regarded as one of the most promising techniques
for poorly-soluble active pharmaceutical ingredients (API). However, the thermodynamic …

Tailoring Chlorthalidone Aqueous Solubility by Cocrystallization: Stability and Dissolution Behavior of a Novel Chlorthalidone-Caffeine Cocrystal

C Rodríguez-Ruiz, P Montes-Tolentino… - Pharmaceutics, 2022 - mdpi.com
A cocrystal of the antihypertensive drug chlorthalidone (CTD) with caffeine (CAF) was
obtained (CTD-CAF) by the slurry method, for which a 2: 1 stoichiometric ratio was found by …

Effects of hypromellose acetate succinate on recrystallization inhibition, miscibility, and dissolution enhancement of baloxavir marboxil solid dispersions

L Wang, H Wu, Z Wang, Z Ding, Y Zhao, S Li… - International Journal of …, 2024 - Elsevier
Solid dispersions (SDs) have emerged as a promising strategy to enhance the solubility and
bioavailability of poorly soluble active pharmaceutical ingredients. However, SDs tend to …

Formulation and In Vitro Characterization of a Vacuum-Dried Drug–Polymer Thin Film for Intranasal Application

D Inoue, A Yamashita, H To - Polymers, 2022 - mdpi.com
Intranasal drug applications show significant therapeutic potential for diverse
pharmaceutical modalities. Because the formulation applied to the nasal cavity is …

Sodium alginate based fast swelling nanogels for solubility enhancement of chlorthalidone; synthesis, characterization and biosafety evaluation

SF Badshah, O Abdullah, KU Khan… - Biomedical …, 2024 - iopscience.iop.org
Purpose of the study was to enhance the solubility of chlorthalidone, poorly soluble diuretic
that has been the used for lowering high blood pressure for the past half-century. Solubility …

The role of glycyrrhizic acid in colloidal phenomena of supersaturation drug delivery systems containing the antifungal drug griseofulvin

MT Franca, TM Marcos, PFA Costa, AP Gerola… - Journal of Molecular …, 2020 - Elsevier
The ability of carriers to inhibit precipitation may determine supersaturating drug delivery
systems capability of improving poorly soluble drugs bioavailability. It was hypothesized that …

Polymer/lipid interplay in altering in vitro supersaturation and plasma concentration of a model poorly soluble drug

R Peng, J Huang, L He, L Zhao, C Wang, W Wei… - European Journal of …, 2020 - Elsevier
Supersaturation drug delivery system (SDDS) based on amorphous solid dispersion (ASD)
is a widely used strategy to improve oral absorption of poorly water-soluble drugs by …