… hour release formulation of the poorly soluble drug silybin based on porous silica nanoparticles: in vitro release kinetics and in vitro/in vivo correlations in beagle dogs

X Cao, W Deng, M Fu, Y Zhu, H Liu, L Wang… - European Journal of …, 2013 - Elsevier
… The objective of this study was to prepare a 72 h-release formulation of silybin (72 h-SLB) …
and porous silica nanoparticles (PSNs) and to investigate the in vitro/in vivo correlations (…

Strategies for MR Formulation Development: Mesoporous Silica

GK Eleftheriadis, E Kontogiannidou… - … Formulations, 2022 - Wiley Online Library
Seventy- twohour release formulation of the poorly soluble drug silybin based on porous
silica nanoparticles: in vitro release kinetics and in vitro/in vivo correlations in beagle

Recent advances in the nanotechnology-based drug delivery of Silybin

Y Wang, L Zhang, Q Wang… - … nanotechnology, 2014 - ingentaconnect.com
… , et al., Seventy-two-hour release formulation of the poorly soluble drug silybin based on
porous silica nanoparticles: In vitro release kinetics and in vitro/in vivo correlations in beagle

[PDF][PDF] Drug Delivery Strategies for Poorly Water-Soluble Silymarin

A Di Costanzo, R Angelico - 2020 - videleaf.com
… After oral administration in beagle dogs of drug entrapped in … Based on the analysis of drug
release profiles in vitro, the … synthesis of monodispersed Porous Silica Nanoparticles (PSNs) …

[HTML][HTML] Formulation strategies for enhancing the bioavailability of silymarin: the state of the art

A Di Costanzo, R Angelico - Molecules, 2019 - mdpi.com
… have been used to optimize silymarin solubility. Most of the … After oral administration in
beagle dogs of drug entrapped in … the synthesis of monodispersed porous silica NPs (PSNs) by …

[HTML][HTML] Synthesis of Pore-Size-Tunable Mesoporous Silica Nanoparticles by Simultaneous Sol-Gel and Radical Polymerization to Enhance Silibinin Dissolution

M Shafiee, S Abolmaali, M Abedanzadeh… - Iranian Journal of …, 2021 - ncbi.nlm.nih.gov
… is low due to poor water solubility. This study aimed to … sustained release of silymarin from
porous silica nanoparticles (… Our in vitro release study indicated that, unlike free SBN, which …

Advanced nanotechnologies for enhancing the bioavailability of silymarin: a state of the art

A Di Costanzo, R Angelico - 2019 - preprints.org
… bioavailability 130 of poorly water-soluble drug compounds, … After oral 326 administration
in beagle dogs of SIL entrapped … nanometer- 704 sized pores with sodium carbonate solution. …

In vitro & in vivo correlation of release behavior of andrographolide from silica and PEG assisted silica gel matrix

S Chakraborty, S Biswas, B Sa, S Das, R Dey - Colloids and Surfaces A …, 2014 - Elsevier
… the nano porous silica as well as PEG modified silica matrix … For all the formulations Level A
in vitro-in vivo correlation (IVIVC) … Relationship between fraction dissolved in vitro vs. fraction …

[HTML][HTML] A review ofin vitrodrug release test methods for nano-sized dosage forms

S D'Souza - Advances in pharmaceutics, 2014 - hindawi.com
… , and establishment of an in vitro in vivo correlation (IVIVC). … in vivo release from beagle dogs
with in vitro release assessed … et al., “In vitro release and in vitroin vivo correlation for silybin

In vitro nanodelivery of silibinin as an anticancer drug under pH response

JM Tan, G Karthivashan, P Arulselvan… - Journal of Drug Delivery …, 2014 - Elsevier
… Yu, Seventy-two-hour release formulation of the poorly soluble drug silybin based on
porous silica nanoparticles: in vitro release kinetics and release kinetics and in vitro/in vivo