Evidence map›Paper›PMID 33116481›Full record

ArticleInternational journal of nanomedicine2020

Biomimetic Synthesis and Evaluation of Interconnected Bimodal Mesostructured MSF@Poly(Ethyleneimine)s for Improved Drug Loading and Oral Adsorption of the Poorly Water-Soluble Drug, Ibuprofen.

Wei Xin, Yumei Wang, Xianmou Guo, Kaijun Gou, Jing Li, Sanming Li, Lin Zhao, Heran Li

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Wei XinSchool of Pharmacy, China Medical University, Shenyang 110122, People's Republic of China.
Yumei WangSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
Xianmou GuoSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
Kaijun GouSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
Jing LiSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
Sanming LiSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
Lin ZhaoSchool of Pharmacy, China Medical University, Shenyang 110122, People's Republic of China.
Heran LiSchool of Pharmacy, China Medical University, Shenyang 110122, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of this study was to improve the oral bioavailability and anti-inflammatory activity of the poorly soluble drug ibuprofen (IBU) by employing a new kind of poly(ethyleneimine)s (PEIs)-based mesocellular siliceous foam (MSF) called B-BMSF@PEI as drug carrier.

methodsB-BMSF@PEI was biomimetically synthesized by using PEIs as templates, catalysts and scaffolds under ambient conditions, and the structural characteristics, including size, morphology, mesoscopic structure and pore properties, were estimated by TEM, SEM, FTIR and N

resultsThe results demonstrated that B-BMSF@PEI was a meso-meso porous silica material with foam appearance. It consisted of uniform spherical cells (40 nm) with interconnected pore networks. IBU can be successfully loaded into B-BMSF@PEI with high efficiency (as high as 39.53%), and crystal IBU was effectively converted to an amorphous state during this process. Benefiting from the great architectures of B-BMSF@PEI, IBU/B-BMSF@PEI performed good wetting property and significantly improved the dissolution rate in both simulated gastric fluid (SGF) and simulated intestinal fluid (SIF). Notably, IBU exhibited very satisfactory relative bioavailability (681.4%) and anti-inflammatory effects (the inhibition rates were between the ranges of 113.5% to 1504.3%).

conclusionB-BMSF@PEI with bimodal mesoporous system and interconnected nanopores was obtained owing to the dynamic self-assembly functions of PEIs. It had superiority in drug loading and could improve the oral adsorption of ibuprofen to a satisfactory level.

Indexed as

Administration, OralAdsorptionAnimalsAnti-Inflammatory Agents, Non-SteroidalAziridinesBiological AvailabilityBiomimeticsDrug CarriersDrug LiberationIbuprofenMaleMiceNanoporesPorosityRats, Sprague-DawleySilicon DioxideAnti-Inflammatory Agents, Non-SteroidalAziridinesDrug CarriersIbuprofenSilicon DioxideWaterbimodal mesostructuredbioavailabilitybiomimetic synthesisibuprofenMSF

Identifiers

PMID33116481
PMCPMC7547139

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.