Evidence map›Paper›PMID 41741729›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2026

A comprehensive review on thermo-responsive targeted and functional therapy for management of rheumatoid arthritis.

Huma Hameed, Syed Sharf Ud Din, Muhammad Zaman, Muhammad Ahsan Waqar, Kainat Fatima, Abdullah Ashraf, Huzaifa Malik, Ahmad Salawi

Abstract readReview
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In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 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

8 authors.

Huma HameedFaculty of Pharmaceutical Sciences, University of Central Punjab, Lahore, 54000, Pakistan. huma.hameed@ucp.edu.pk.
Syed Sharf Ud DinFaculty of Pharmaceutical Sciences, University of Central Punjab, Lahore, 54000, Pakistan.
Muhammad ZamanFaculty of Pharmaceutical Sciences, University of Central Punjab, Lahore, 54000, Pakistan.
Muhammad Ahsan WaqarDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Lahore University of Biological & Applied Sciences, Lahore, Pakistan.
Kainat FatimaFaculty of Pharmaceutical Sciences, University of Central Punjab, Lahore, 54000, Pakistan.
Abdullah AshrafFaculty of Pharmaceutical Sciences, University of Central Punjab, Lahore, 54000, Pakistan.
Huzaifa MalikFaculty of Pharmaceutical Sciences, University of Central Punjab, Lahore, 54000, Pakistan.
Ahmad SalawiDepartment of Pharmaceutics, College of Pharmacy, Jazan University, 45142, Jazan, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most common autoimmune illness in both developed and under developed countries is rheumatoid arthritis (RA). In the past, RA could not be effectively treated with any existing strategies. However, new medications and therapeutic approaches have been created to combat this condition in the present day as a result of advancements in drug delivery science. Numerous advancements have been made in the therapy formulations for RA that are currently on the market in the last few years. One well-known medication for the treatment of RA is methotrexate (MTX). However, most current treatment formulations have several adverse effects and are unable to completely alleviate all RA symptoms. Combination therapy for the treatment of RA may be more successful than MTX therapy alone in addressing such problems. We discovered that MTX plus infliximab (INF), golimumab (GOL), leflunomide (LEF), folic acid (FA), and azathioprine was more successful than MTX alone because it had less adverse effects and a lower risk of RA relapses. MTX monotherapy has been shown to be less effective than combinations with one or more drugs. We examined the many injectable treatments for RA, focusing on thermo-responsive targeted drug delivery systems as cutting-edge means of delivering MTX, either alone or in conjunction with other treatments. Thermo-responsive in situ hydrogel-based injectables in latest drug delivery systems have the potential to address many of the challenges related to RA treatment and therapy.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidDrug Delivery SystemsAnimalsDrug Therapy, CombinationHumansMethotrexateTemperatureAntirheumatic AgentsMethotrexateHydrogelInjectableRheumatoid arthritisTargetedThermo-responsive

Identifiers

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.