Evidence map›Paper›PMID 33886076›Full record

ArticleDrug delivery and translational research2022

Dermal delivery of amitriptyline for topical analgesia.

Chin-Ping Kung, Bruno C Sil, Yanling Zhang, Jonathan Hadgraft, Majella E Lane, Bhumik Patel, Renée McCulloch

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Drug delivery and translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07214181 (Topical Amitriptyline 1% Gel for the Treatment of Burning Mouth Syndrome), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 46% 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.

NCT07214181 completednot on this mapstarted 2024, after this paper: background citation

Topical Amitriptyline 1% Gel for the Treatment of Burning Mouth Syndrome

Typeobservational_patient_registrySponsorUniversidad de MurciaRan2024 to 2025Enrolled30ConditionsBurning Mouth Syndrome, StomatodyniaArmsTopical amitriptyline 1% gel
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Observational
  2. Review
  3. Review
  4. Review
  5. Article
  6. 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

7 authors at 3 institutions in 1 country.

Chin-Ping KungUCL School of Pharmacy, 29-39 Brunswick Square, London, WC1N 1AX, UK. c.kung@ucl.ac.uk.
Bruno C SilLondon Metropolitan University, 166-220 Holloway Road, London, N7 8DB, UK.
Yanling ZhangUCL School of Pharmacy, 29-39 Brunswick Square, London, WC1N 1AX, UK.
Jonathan HadgraftUCL School of Pharmacy, 29-39 Brunswick Square, London, WC1N 1AX, UK.
Majella E LaneUCL School of Pharmacy, 29-39 Brunswick Square, London, WC1N 1AX, UK.
Bhumik PatelGreat Ormond Street Hospital for Children, Great Ormond Street, London, WC1N 3JH, UK.
Renée McCullochGreat Ormond Street Hospital for Children, Great Ormond Street, London, WC1N 3JH, UK.
University College London · GBGreat Ormond Street Hospital · GBLondon Metropolitan University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amitriptyline, administered orally, is currently one of the treatment options for the management of neuropathic pain and migraine. Because of the physicochemical properties of the molecule, amitriptyline is also a promising candidate for delivery as a topical analgesic. Here we report the dermal delivery of amitriptyline from a range of simple formulations. The first stage of the work required the conversion of amitriptyline hydrochloride to the free base form as confirmed by nuclear magnetic resonance (NMR). Distribution coefficient values were measured at pH 6, 6.5, 7, and 7.4. Solubility and stability of amitriptyline were assessed prior to conducting in vitro permeation and mass balance studies. The compound demonstrated instability in phosphate-buffered saline (PBS) dependent on pH. Volatile formulations comprising of isopropyl alcohol (IPA) and isopropyl myristate (IPM) or propylene glycol (PG) were evaluated in porcine skin under finite dose conditions. Compared with neat IPM, the IPM:IPA vehicles promoted 8-fold and 5-fold increases in the amount of amitriptyline that permeated at 24 h. Formulations containing PG also appear to be promising vehicles for dermal delivery of amitriptyline, typically delivering higher amounts of amitriptyline than the IPM:IPA vehicles. The results reported here suggest that further optimization of topical amitriptyline formulations should be pursued towards development of a product for clinical investigational studies.

Indexed as

AnalgesiaSkin AbsorptionAdministration, CutaneousAmitriptylineAnalgesicsAnimalsExcipientsPropylene GlycolSkinSwineAmitriptylineAnalgesicsExcipientsPropylene GlycolAmitriptylineCo-solvent systemPenetration enhancementSkin permeationTopical analgesic

Identifiers

PMID33886076
PMCPMC8888505
OpenAlexW3155300610

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.