Evidence map›Paper›PMID 37513879›Full record

ReviewPharmaceuticals (Basel, Switzerland)2023

Smart Strategies to Overcome Drug Delivery Challenges in the Musculoskeletal System.

Brandon Vorrius, Zhen Qiao, Jonathan Ge, Qian Chen

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.4field-weighted citation impact, top 5% 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.

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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Stem cell therapies in the clinic.Bioengineering & translational medicine · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. 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

4 authors at 1 institution in 1 country.

Brandon VorriusLaboratory of Molecular Biology and Nanomedicine, Department of Orthopaedics, Alpert Medical School of Brown University/Rhode Island Hospital, Providence, RI 02903, USA.
Zhen QiaoLaboratory of Molecular Biology and Nanomedicine, Department of Orthopaedics, Alpert Medical School of Brown University/Rhode Island Hospital, Providence, RI 02903, USA.
Jonathan GeLaboratory of Molecular Biology and Nanomedicine, Department of Orthopaedics, Alpert Medical School of Brown University/Rhode Island Hospital, Providence, RI 02903, USA.
Qian ChenLaboratory of Molecular Biology and Nanomedicine, Department of Orthopaedics, Alpert Medical School of Brown University/Rhode Island Hospital, Providence, RI 02903, USA.ORCID 0000-0003-4406-5618
Brown University · US

Funding

Pilot Projects ProgramP30GM122732 · NIGMS · RHODE ISLAND HOSPITAL · PI CRISCO, JOSEPH J · 2017 to 2021
$6.6M
Predoctoral Training in the Molecular Biology of AgingT32AG041688 · NIA · BROWN UNIVERSITY · PI NICOLA NERETTI, John M Sedivy · 2012 to 2026
$3.5M
Single-Cell Transposon Activation in the CNS during AD Progression: Sex-dependent MechanismsR01AG080141 · NIA · RHODE ISLAND HOSPITAL · PI QIAN CHEN · 2023 to 2026
$2.9M
Repressing Retrotransposon LINE-1: New Concepts for Osteoarthritis TreatmentR61AR076807 · NIAMS · RHODE ISLAND HOSPITAL · PI CHEN, QIAN · 2019 to 2020
$1.2M
Repressing Retrotransposon LINE-1: New Concepts for Osteoarthritis TreatmentR33AR076807 · NIAMS · RHODE ISLAND HOSPITAL · PI CHEN, QIAN · 2021 to 2021
$397k
Developing Nanopieces, a Platform RNAi Delivery Technology for Treatment of Multiple DiseasesR41TR002298 · NCATS · NANODE THERAPEUTICS, INC. · PI CHEN, QIAN · 2020 to 2020
$325k
NCATS NIH HHS R41 TR002298NCATS NIH HHS R41TR002298NIAMS NIH HHS R33 AR076807NIAMS NIH HHS R61 AR076807NIA NIH HHS R01 AG080141NIA NIH HHS T32 AG041688NIGMS NIH HHS P30 GM122732NIGMS NIH HHS P30GM122732
6 · The paper itself

Abstract

The musculoskeletal system (MSKS) is composed of specialized connective tissues including bone, muscle, cartilage, tendon, ligament, and their subtypes. The primary function of the MSKS is to provide protection, structure, mobility, and mechanical properties to the body. In the process of fulfilling these functions, the MSKS is subject to wear and tear during aging and after injury and requires subsequent repair. MSKS diseases are a growing burden due to the increasing population age. The World Health Organization estimates that 1.71 billon people suffer from MSKS diseases worldwide. MSKS diseases usually involve various dysfunctions in bones, muscles, and joints, which often result in pain, disability, and a decrease in quality of life. The most common MSKS diseases are osteoporosis (loss of bone), osteoarthritis (loss of cartilage), and sarcopenia (loss of skeletal muscle). Because of the disease burden and the need for treatment, regenerative drug therapies for MSKS disorders are increasingly in demand. However, the difficulty of effective drug delivery in the MSKS has become a bottleneck for developing MSKS therapeutics. The abundance of extracellular matrix and its small pore size in the MSKS present a formidable barrier to drug delivery. Differences of vascularity among various MSKS tissues pose complications for drug delivery. Novel strategies are necessary to achieve successful drug delivery in different tissues composing the MSKS. Those considerations include the route of administration, mechanics of surrounding fluids, and biomolecular interactions, such as the size and charge of the particles and targeting motifs. This review focuses on recent advances in challenges to deliver drugs to each tissue of the MSKS, current strategies of drug delivery, and future ideas of how to overcome drug delivery challenges in the MSKS.

Indexed as

bonecartilagedrug deliverymusclemusculoskeletal systemtissue barriers

Identifiers

PMID37513879
PMCPMC10383421
OpenAlexW4383536239

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.