Evidence map›Paper›PMID 34283375›Full record

ArticlePharmacological reports : PR2021

Pharmacokinetics and tissue distribution of hydrazinocurcumin in rats.

Satyavert, Sumeet Gupta, Hira Choudhury, Shery Jacob, Anroop B Nair, Meenakshi Dhanawat, Kavita Munjal

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Pharmacological reports : PR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. QbD driven targeted pulmonary delivery of dexamethasone-loaded chitosan microspheres: Biodistribution and pharmacokinetic study.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
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

7 authors at 4 institutions in 4 countries.

SatyavertDepartment of Pharmaceutical Sciences, M. M. College of Pharmacy, M. M. Deemed To Be University, Mullana, Ambala, Haryana, India.
Sumeet GuptaDepartment of Pharmaceutical Sciences, M. M. College of Pharmacy, M. M. Deemed To Be University, Mullana, Ambala, Haryana, India. sumeetgupta25@gmail.com.ORCID http://orcid.org/0000-0003-2980-7791
Hira ChoudhurySchool of Pharmacy, International Medical University, Bukit Jalil, 57000, Kuala Lumpur, Malaysia.
Shery JacobDepartment of Pharmaceutical Sciences, College of Pharmacy, Gulf Medical University, 4184, Ajman, United Arab Emirates.
Anroop B NairDepartment of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa, 31982, Saudi Arabia.
Meenakshi DhanawatDepartment of Pharmaceutical Sciences, M. M. College of Pharmacy, M. M. Deemed To Be University, Mullana, Ambala, Haryana, India.
Kavita MunjalDepartment of Pharmaceutical Sciences, M. M. College of Pharmacy, M. M. Deemed To Be University, Mullana, Ambala, Haryana, India.
Gulf Medical University · AEIMU University · MYKing Faisal University · SAMVN University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurcumin, a natural polyphenol from Curcuma longa, is known to possess diversified pharmacological roles including anti-inflammatory, antioxidant, antiproliferative and antiangiogenic properties; however, its bioavailability is severely limited due to its poor solubility, poor absorption, rapid metabolism, and significant elimination. Hydrazinocurcumin (HZC), a novel analogue of curcumin has been reported to overcome the limitations of curcumin and also possesses multiple pharmacological activities. The present study aimed to evaluate the unexplored pharmacokinetic profile of this agent in experimental rats.

methodsDrug formulations were administered to the experimental animals via oral, intravenous and intraperitoneal routes. Blood samples were collected at different pre-determined time intervals to determine the pharmacokinetic parameters. To understand the biodistribution profile of HCZ, tissue samples were isolated from different groups of Sprague-Dawley rats at different time points. The pharmacokinetic parameters of HZC were evaluated after administration through oral (100 mg/kg), intraperitoneal (100 mg/kg) and intravenous (10 mg/kg) routes.

resultsSignificantly (p < 0.05) higher total AUC along with maximum concentration were evident with intraperitoneal administration when compared to the results of oral administration at a similar dose. In addition, shorter time to peak was observed with intraperitoneal administration. These results revealed a faster rate and longer duration of absorption with intraperitoneal administration, which further resulted in enhanced absolute bioavailability of HZC (29.17%) when compared to 5.1% upon oral dosing. The obtained data from the pharmacokinetic study indicated that HZC was instantaneously distributed and moderately eliminated from body fluids.

conclusionBased on the findings, it could be concluded that absorption of HZC is much higher via intraperitoneal route of administration compared to the oral administration.

Indexed as

Administration, IntravenousAdministration, OralAnimalsAntioxidantsArea Under CurveBiological AvailabilityCurcuminHydrazinesInjections, IntraperitonealRatsRats, Sprague-DawleyTissue DistributionAntioxidantsCurcuminHydrazineshydrazinocurcuminHydrazinocurcuminIntraperitoneal administrationIntravenousOral bioavailabilityPharmacokineticsTissue distribution

Identifiers

PMID34283375
OpenAlexW3186274567

What OpenQuestion holds

Textmetadata
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.