Evidence map›Paper›PMID 39179013›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2024

Identification of formulation parameters that affect the analgesic efficacy of ProGel-Dex - A thermoresponsive polymeric dexamethasone prodrug for chronic arthritis pain relief.

Xin Wei, Gang Zhao, Ningrong Chen, Xiaoke Xu, Haochen Jiang, Daniel Tran, Evan Glissmeyer, Mary B Goldring, Steven R Goldring, Dong Wang

Abstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

10 authors.

Xin WeiDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Gang ZhaoEnsign Pharmaceutical, Inc., Omaha, NE 68106, USA.
Ningrong ChenDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Xiaoke XuDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Haochen JiangDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Daniel TranEnsign Pharmaceutical, Inc., Omaha, NE 68106, USA.
Evan GlissmeyerEnsign Pharmaceutical, Inc., Omaha, NE 68106, USA.
Mary B GoldringHospital for Special Surgery, New York, NY 10021, USA.
Steven R GoldringEnsign Pharmaceutical, Inc., Omaha, NE 68106, USA; Hospital for Special Surgery, New York, NY 10021, USA.
Dong WangDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, 68198, USA; Ensign Pharmaceutical, Inc., Omaha, NE 68106, USA; Department of Orthopaedic Surgery & Rehabilitation, College of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA. Electronic address: dwang@unmc.edu.

Funding

Nonaddictive opioid prodrug nanomedicine for musculoskeletal painR01AR080500 · NIAMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Dong Wang · 2022 to 2026
$2.3M
ProGel Technology for Better Management of Osteoarthritis PainR44DA051278 · NIDA · ENSIGN PHARMACEUTICAL, INC · PI GOLDRING, STEVEN · 2020 to 2022
$1.9M
NIAMS NIH HHS R01 AR080500NIDA NIH HHS R44 DA051278
6 · The paper itself

Abstract

The relief of joint pain is one of the main objectives in the clinical management of arthritis. Although significant strides have been made in improving management of rheumatoid and related forms of inflammatory arthritis, there are still major unmet needs for therapies that selectively provide potent, sustained and safe joint pain relief, especially among patients with osteoarthritis (OA), the most common form of arthritis. We have recently developed ProGel-Dex, an N-(2-hydroxypropyl) methacrylamide (HPMA) copolymer-based thermoresponsive dexamethasone (Dex) prodrug, which forms a hydrogel upon intra-articular administration and provides sustained improvement in pain-related behavior and inflammation in rodent models of arthritis. The focus of the present study was to investigate the impact of ProGel-Dex formulation parameters on its physicochemical properties and in vivo efficacy. The results of this study provide essential knowledge for the future design of ProGel-Dex that can provide more effective, sustained and safe relief of joint pain and inflammation.

Indexed as

DexamethasoneProdrugsAnalgesicsAnimalsArthritis, ExperimentalChronic PainHumansHydrogelsMaleMiceOsteoarthritisPolymersRatsAnalgesicsDexamethasoneHydrogelsPolymersProdrugsDexamethasoneHydrogelOsteoarthritisPainProdrugThermoresponsive

Identifiers

PMID39179013
PMCPMC11687284

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.