Evidence map›Paper›PMID 35956734›Full record

ArticlePolymers2022

A QbD Approach to Design and to Optimize the Self-Emulsifying Resveratrol-Phospholipid Complex to Enhance Drug Bioavailability through Lymphatic Transport.

Syed Abul Layes Gausuzzaman, Mithun Saha, Shahid Jaman Dip, Shaiful Alam, Arup Kumar, Harinarayan Das, Shazid Md Sharker, Md Abdur Rashid, Mohsin Kazi, Hasan Mahmud Reza

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 25 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Syed Abul Layes GausuzzamanDepartment of Pharmaceutical Sciences, North South University, Dhaka 1229, Bangladesh.
Mithun SahaDepartment of Pharmaceutical Sciences, North South University, Dhaka 1229, Bangladesh.ORCID 0000-0002-8541-3036
Shahid Jaman DipDepartment of Pharmaceutical Sciences, North South University, Dhaka 1229, Bangladesh.
Shaiful AlamDepartment of Pharmaceutical Sciences, North South University, Dhaka 1229, Bangladesh.
Arup KumarMaterials Science Division, Atomic Energy Centre, 4 Kazi Nazrul Islam Avenue, Shahbagh, Dhaka 1000, Bangladesh.
Harinarayan DasMaterials Science Division, Atomic Energy Centre, 4 Kazi Nazrul Islam Avenue, Shahbagh, Dhaka 1000, Bangladesh.
Shazid Md SharkerDepartment of Pharmaceutical Sciences, North South University, Dhaka 1229, Bangladesh.ORCID 0000-0001-9122-3602
Md Abdur RashidDepartment of Pharmaceutics, College of Pharmacy, King Khalid University, Guraiger, Abha 62529, Saudi Arabia.ORCID 0000-0001-9404-5186
Mohsin KaziDepartment of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-5611-0378
Hasan Mahmud RezaDepartment of Pharmaceutical Sciences, North South University, Dhaka 1229, Bangladesh.ORCID 0000-0003-3287-942X
North South University · BDBangladesh Atomic Energy Commission · BDKing Saud University · SAQueensland University of Technology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Despite having profound therapeutic value, the clinical application of resveratrol is restrained due to its <1% bioavailability, arising from the extensive fast-pass effect along with enterohepatic recirculation. This study aimed to develop a self-emulsifying formulation capable of increasing the bioavailability of resveratrol via lymphatic transport. Methods: The resveratrol−phospholipid complex (RPC) was formed by the solvent evaporation method and characterized by FTIR, DSC, and XRD analyses. The RPC-loaded self-emulsifying drug delivery system (SEDDS) was designed, developed, and optimized using the QbD approach with an emphasis on resveratrol transport through the intestinal lymphatic pathway. The in vivo pharmacokinetic study was investigated in male Wister Albino rats. Results: The FTIR, DSC, and XRD analyses confirmed the RPC formation. The obtained design space provided robustness of prediction within the 95% prediction interval to meet the CQA specifications. An optimal formulation (desirability value of 7.24) provided Grade-A self-emulsion and exhibited a 48-fold bioavailability enhancement compared to the pure resveratrol. The cycloheximide-induced chylomicron flow blocking approach demonstrated that 91.14% of the systemically available resveratrol was transported through the intestinal lymphatic route. Conclusions: This study suggests that an optimal self-emulsifying formulation can significantly increase the bioavailability of resveratrol through lymphatic transport to achieve the desired pharmacological effects.

Indexed as

bioavailabilitychylomicron flow blocking approachlymphatic drug transportquality by designresveratrol–phospholipid complexself-emulsifying drug delivery system

Identifiers

PMID35956734
PMCPMC9371077
OpenAlexW4290759731

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Registered trials

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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.