Evidence map›Paper›PMID 31529175›Full record

ArticleAAPS PharmSciTech2019

Physicochemical Profiling of Baicalin Along with the Development and Characterization of Cyclodextrin Inclusion Complexes.

Géza Jakab, Dóra Bogdán, Károly Mazák, Ruth Deme, Zoltán Mucsi, István M Mándity, Béla Noszál, Nikolett Kállai-Szabó, István Antal

Abstract read
In one paragraph

Article in AAPS PharmSciTech, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Drug Candidates for Autoimmune Diseases.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  17. An ultrasensitive high-performance baicalin sensor based on CSensors and actuators. B, Chemical · 2022
    Article
  18. Review
  19. Review
  20. TopicalPharmaceutics · 2021
    Article
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

9 authors.

Géza JakabDepartment of Pharmaceutics, Semmelweis University, Hőgyes E. Street 7-9, Budapest, 1092, Hungary.
Dóra BogdánDepartment of Organic Chemistry, Semmelweis University, Hőgyes E. Street 7-9, Budapest, 1092, Hungary.
Károly MazákDepartment of Pharmaceutical Chemistry, Semmelweis University, Hőgyes E. Street 7-9, Budapest, 1092, Hungary.
Ruth DemeDepartment of Organic Chemistry, Semmelweis University, Hőgyes E. Street 7-9, Budapest, 1092, Hungary.
Zoltán MucsiFemtonics Ltd., Tűzoltó Street 59, Budapest, 1094, Hungary.
István M MándityDepartment of Organic Chemistry, Semmelweis University, Hőgyes E. Street 7-9, Budapest, 1092, Hungary.
Béla NoszálDepartment of Pharmaceutical Chemistry, Semmelweis University, Hőgyes E. Street 7-9, Budapest, 1092, Hungary.
Nikolett Kállai-SzabóDepartment of Pharmaceutics, Semmelweis University, Hőgyes E. Street 7-9, Budapest, 1092, Hungary.
István AntalDepartment of Pharmaceutics, Semmelweis University, Hőgyes E. Street 7-9, Budapest, 1092, Hungary. antal.istvan@pharma.semmelweis-univ.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Baicalin is a flavone glycoside extracted from Scutellaria baicalensis, a traditional Chinese herbal medicine. Numerous pharmacological effects of baicalin were reported (e.g. antioxidant, anxiolytic); nevertheless, the most important physicochemical properties influencing the pharmacokinetic behaviour and the concomitant oral bioavailability have not yet been described in a comprehensive study. The aim of this project was to characterize the acid-base, lipophilicity, biorelevant solubility and permeability properties of the drug substance and providing scientific data to support the dosage form design. Another important objective was the comparative evaluation of six various baicalin-cyclodextrin (CD) inclusion complexes along with the creation of a suitable Drug Delivery System (DDS) for this BCS IV drug. Biorelevant profiling was carried out by NMR-pH titrations, saturation shake-flask and distribution coefficients (logP) measurements, while CD inclusion studies were fulfilled by experimental methods (phase solubility,

Indexed as

Antineoplastic Agents, PhytogenicBiological AvailabilityCyclodextrinsDrug Delivery SystemsFlavonoidsLipidsMagnetic Resonance SpectroscopyModels, MolecularPermeabilitySolubilityThermodynamicsAntineoplastic Agents, PhytogenicbaicalinCyclodextrinsFlavonoidsLipidsbaicalincomputational modellingcyclodextrinsphysicochemical analysissolubility enhancement

Identifiers

PMID31529175
PMCPMC6746686

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.