Evidence map›Paper›PMID 36903399›Full record

ArticleMolecules (Basel, Switzerland)2023

Enhanced Drug Delivery System Using Mesenchymal Stem Cells and Membrane-Coated Nanoparticles.

Shubham Joshi, Sarah Allabun, Stephen Ojo, Mohammed S Alqahtani, Piyush Kumar Shukla, Mohamed Abbas, Chitapong Wechtaisong, Hussain M Almohiy

Full text read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  13. Current advancements in nanotechnology for stem cells.International journal of surgery (London, England) · 2024
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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.

Shubham JoshiDepartment of Computer Engineering, SVKM'S NMIMS Mukesh Patel School of Technology Management and Engineering, Shirpur 425405, Maharashtra, India.ORCID 0000-0003-3815-1261
Sarah AllabunDepartment of Medical Education, College of Medicine, Princess Nourah bint Abdulrahman University, Riyadh 11671, Saudi Arabia.ORCID 0000-0003-4395-1343
Stephen OjoElectrical and Computer Engineering, College of Engineering, Springdale, 316 Boulevard, Anderson, SC 29621, USA.ORCID 0000-0002-2383-621X
Mohammed S AlqahtaniRadiological Sciences Department, College of Applied Medical Sciences, King Khalid University, Abha 61421, Saudi Arabia.ORCID 0000-0001-7425-3578
Piyush Kumar ShuklaDepartment of Computer Science and Engineering, University Institute of Technology, Rajiv Gandhi Proudyogiki Vishwavidyalaya (Technological University of Madhya Pradesh), Bhopal 462033, Madhya Pradesh, India.ORCID 0000-0002-3715-3882
Mohamed AbbasElectrical Engineering Department, College of Engineering, King Khalid University, Abha 61421, Saudi Arabia.ORCID 0000-0002-3141-2900
Chitapong WechtaisongSchool of Telecommunication Engineering, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand.
Hussain M AlmohiyRadiological Sciences Department, College of Applied Medical Sciences, King Khalid University, Abha 61421, Saudi Arabia.

Funding

Princess Nourah bint Abdulrahman University 4/3/89
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) have newly developed as a potential drug delivery system. MSC-based drug delivery systems (MSCs-DDS) have made significant strides in the treatment of several illnesses, as shown by a plethora of research. However, as this area of research rapidly develops, several issues with this delivery technique have emerged, most often as a result of its intrinsic limits. To increase the effectiveness and security of this system, several cutting-edge technologies are being developed concurrently. However, the advancement of MSC applicability in clinical practice is severely hampered by the absence of standardized methodologies for assessing cell safety, effectiveness, and biodistribution. In this work, the biodistribution and systemic safety of MSCs are highlighted as we assess the status of MSC-based cell therapy at this time. We also examine the underlying mechanisms of MSCs to better understand the risks of tumor initiation and propagation. Methods for MSC biodistribution are explored, as well as the pharmacokinetics and pharmacodynamics of cell therapies. We also highlight various promising technologies, such as nanotechnology, genome engineering technology, and biomimetic technology, to enhance MSC-DDS. For statistical analysis, we used analysis of variance (ANOVA), Kaplan Meier, and log-rank tests. In this work, we created a shared DDS medication distribution network using an extended enhanced optimization approach called enhanced particle swarm optimization (E-PSO). To identify the considerable untapped potential and highlight promising future research paths, we highlight the use of MSCs in gene delivery and medication, also membrane-coated MSC nanoparticles, for treatment and drug delivery.

Indexed as

Mesenchymal Stem CellsNanoparticlesCytoplasmDrug Delivery SystemsTissue Distributiondrug delivery systemenhanced particle swarm optimization (E-PSO)mesenchymal stem cell (MSC)nanoparticlespharmacodynamicspharmacokinetics

Identifiers

PMID36903399
PMCPMC10004171

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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.