[HTML][HTML] Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability

P Khadka, J Ro, H Kim, I Kim, JT Kim, H Kim… - Asian journal of …, 2014 - Elsevier
Pharmaceutical particle technology is employed to improve poor aqueous solubility of drug
compounds that limits in vivo bioavailability owing to their low dissolution rate in the …

Hydrophobic ion pairing: encapsulating small molecules, peptides, and proteins into nanocarriers

KD Ristroph, RK Prud'homme - Nanoscale advances, 2019 - pubs.rsc.org
Hydrophobic ion pairing has emerged as a method to modulate the solubility of charged
hydrophilic molecules ranging in class from small molecules to large enzymes. Charged …

Lipid-based nanovesicles for nanomedicine

N Grimaldi, F Andrade, N Segovia… - Chemical society …, 2016 - pubs.rsc.org
Molecular self-assembly has enabled the fabrication of biologically inspired, advanced
nanostructures as lipid-based nanovesicles (L-NVs). The oldest L-NVs, liposomes, have …

Implications of protein corona on physico-chemical and biological properties of magnetic nanoparticles

MM Yallapu, N Chauhan, SF Othman… - Biomaterials, 2015 - Elsevier
Interaction of serum proteins and nanoparticles leads to a nanoparticle–protein complex
formation that defines the rational strategy for a clinically relevant formulation for drug …

Current advances in the biomedical applications of quantum dots: promises and challenges

N Le, K Kim - International Journal of Molecular Sciences, 2023 - mdpi.com
Quantum dots (QDs) are a type of nanoparticle with exceptional photobleaching-resistant
fluorescence. They are highly sought after for their potential use in various optical-based …

Utilization of nanoemulsions to enhance bioactivity of pharmaceuticals, supplements, and nutraceuticals: Nanoemulsion delivery systems and nanoemulsion excipient …

KO Aboalnaja, S Yaghmoor, TA Kumosani… - Expert opinion on …, 2016 - Taylor & Francis
Introduction: The efficacy of many hydrophobic bioactives (pharmaceuticals, supplements,
and nutraceuticals) is limited due to their relatively low or highly variable bioavailability …

Formulation and optimization of lacidipine loaded niosomal gel for transdermal delivery: in-vitro characterization and in-vivo activity

M Qumbar, SS Imam, J Ali, J Ahmad, A Ali - Biomedicine & …, 2017 - Elsevier
The aim of the present research work is to formulate lacidipine (LAC) loaded niosomes
formulation for the management of hypertension by thin film hydration technique. The …

Cholinium-based ionic liquids as bioinspired hydrotropes to tackle solubility challenges in drug formulation

TE Sintra, DO Abranches, J Benfica, BP Soares… - European Journal of …, 2021 - Elsevier
Hydrotropy is a well-established strategy to enhance the aqueous solubility of hydrophobic
drugs, facilitating their formulation for oral and dermal delivery. However, most hydrotropes …

Polymeric nanomedicines for poorly soluble drugs in oral delivery systems: An update

X Ma, RO Williams III - Journal of pharmaceutical investigation, 2018 - Springer
The field of nanomedicine offers promising new drug delivery systems with enhanced
properties. The literature has reported on the development of various nanomedicines that …

Clozapine loaded nanostructured lipid carriers engineered for brain targeting via nose-to-brain delivery: Optimization and in vivo pharmacokinetic studies

HP Patel, PA Gandhi, PS Chaudhari, BV Desai… - Journal of Drug Delivery …, 2021 - Elsevier
Clozapine is commonly used to treat schizophrenia but it is having issues of low oral
bioavailability (< 27%), degradation in GI environment and high hepatic first-pass …