ArticleBMC veterinary research2025
Enoxolone pharmacokinetics, tissue distribution, and residue depletion in largemouth bass (Micropterus salmoides).
Article in BMC veterinary research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Enoxolone, a hydrolyzed component of Chinese herbal medicine, has shown efficacy against Flavobacterium columnare in largemouth bass (Micropterus salmoides). However, its pharmacokinetics and muscle residue depletion in M. salmoides are not well understood. This study analyzed plasma and tissue samples using High-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) after exposure to 16 mg/L enoxolone. Results indicated a bimodal plasma absorption pattern, with the first peak at 2 h and the highest concentration (Cmax = 44.67 mg/L) at 24 h. The plasma AUC0−24 h was 813.40 mg·h/L, and the MRT was 36 h. Significant accumulation occurred in the kidneys (Cmax = 2223.33 mg/kg, AUC0−24 h = 7268.967 mg·h/L) which is more than other organs. But the Tmax (72 h) and MRT (51 h) is the longest. Muscle residues declined to 0.0164 mg/kg by day 11 post-immersion and the withdrawal time is at least 15 d. Enoxolone concentrations in plasma and tissues reached the MIC within 4–8 h. Acute toxicity tests showed a 96 h LC50 of 12.17 mg/L, with no mortality at concentrations ≤ 50 mg/L within 24 h. Based on these findings, a 4 h immersion at 16 mg/L is recommended for effective F. columnare control, followed by an 15 d withdrawal period to meet food safety standards. This study offers crucial data for optimizing enoxolone use in aquaculture.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.