Evidence map›Paper›PMID 42002281›Full record

ArticleJournal of the American Association for Laboratory Animal Science : JAALAS2026

Onset of Analgesia in Rats (Rattus norvegicus) for Three Buprenorphine Formulations.

Eden D Alamaw, Kenzie E Schwartz, Mingyun Zhang, Benjamin D Franco, Katechan Jampachaisri, Monika K Huss, Cholawat Pacharinsak

Abstract read
In one paragraph

Article in Journal of the American Association for Laboratory Animal Science : JAALAS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Eden D Alamaw1Department of Comparative Medicine, Stanford University, Stanford, California; and.
Kenzie E Schwartz1Department of Comparative Medicine, Stanford University, Stanford, California; and.
Mingyun Zhang1Department of Comparative Medicine, Stanford University, Stanford, California; and.
Benjamin D Franco1Department of Comparative Medicine, Stanford University, Stanford, California; and.
Katechan Jampachaisri2Department of Mathematics, Naresuan University, Phitsanulok, Thailand.
Monika K Huss1Department of Comparative Medicine, Stanford University, Stanford, California; and.
Cholawat Pacharinsak1Department of Comparative Medicine, Stanford University, Stanford, California; and.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extended-release buprenorphine has been extensively used in laboratory animal medicine, yet its onset of analgesia in rats remains largely unexplored. This study aimed to investigate the analgesic onset of 3 different extended-release buprenorphine formulations in rats. Our hypothesis was that the onset of all 3 buprenorphine formulations are comparable and are detectable as early as 5 minutes after administration in rats. Sprague-Dawley rats (both male and female, n = 40) were randomly assigned to 4 treatment groups: (1) saline (1 mL/0.1 kg SC, once); (2) Bup-ER (1.2 mg/kg SC, once); (3) Ethiqa-XR (0.65 mg/kg SC, once); and (4) LAT-Bup (Zorbium, 10 mg/kg transdermal, once). Thermal sensitivity (using a hot plate test) was assessed at time points of 5, 15, 30, 45, 60, 120, 180, and 240 minutes following drug administration. Results were as follows: (1) compared with the saline group, Bup-ER's thermal latency significantly increased at 45 (11.05 ± 1.13), 60 (12.5 ± 1.16), 120 (13.7 ± 1.24), 180 (12.48 ± 0.81), and 240 (11.64 ± 0.7) minutes; (2) Ethiqa-XR's thermal latency significantly increased at 180 (12.01 ± 0.6) and 240 (11.76 ± 0.81) minutes; and (3) LAT-Bup's thermal latency significantly increased at 120 (11.27 ± 1.16), 180 (13.97 ± 1.35), and 240 (14.8 ± 1.26) minutes. There were no differences between sexes. LAT-Bup and Bup-ER provided buprenorphine plasma levels exceeding the purported therapeutic threshold of 1 ng/mL by 5 minutes, while Ethiqa-XR exceeded the threshold at 45 minutes. We concluded that these 3 buprenorphine extended-release formulations did not exhibit a time to onset of analgesia within 5 minutes. This study demonstrates that despite all 3 extended-release formulations reaching a purported plasma therapeutic threshold earlier, the clinical onset of analgesia for the hot plate test was shortest for Bup-ER (45 minutes), followed by LAT-Bup (120 minutes) and Ethiqa-XR (180 minutes) in Sprague-Dawley rats.

Indexed as

Bup-ER, extended-release buprenorphine base lab in polymerEthiqa-XR, buprenorphine extended-release injectable suspensionLAT-Bup, long-acting transdermal buprenorphine solution

Identifiers

PMID42002281
PMCPMC13249297

What OpenQuestion holds

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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.