Evidence map›Paper›PMID 38161204›Full record

ReviewSignal transduction and targeted therapy2024

Multifunctional nanoparticle-mediated combining therapy for human diseases.

Xiaotong Li, Xiuju Peng, Makhloufi Zoulikha, George Frimpong Boafo, Kosheli Thapa Magar, Yanmin Ju, Wei He

Open access · goldAbstract readReview
In one paragraph

Review in Signal transduction and targeted therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed, 1 pooled it
75.3field-weighted citation impact, top 1% 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

122 citing papers in PubMed, 1 synthesis or guideline pooled it, 442 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Supramolecular Degraders: An Emerging Paradigm in Targeted Protein Degradation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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62 more citing papers are in PubMed but not listed here.

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.

Xiaotong Li *School of Pharmacy, China Pharmaceutical University, Nanjing, 2111198, PR China.
Xiuju Peng *School of Pharmacy, China Pharmaceutical University, Nanjing, 2111198, PR China.
Makhloufi Zoulikha *School of Pharmacy, China Pharmaceutical University, Nanjing, 2111198, PR China.
George Frimpong Boafo *Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, PR China.
Kosheli Thapa Magar *School of Pharmacy, China Pharmaceutical University, Nanjing, 2111198, PR China.
Yanmin JuSchool of Pharmacy, China Pharmaceutical University, Nanjing, 2111198, PR China. juyanmin@cpu.edu.cn.
Wei HeShanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai, 200443, China. weihe@cpu.edu.cn.ORCID 0000-0003-3075-3831
China Pharmaceutical University · CNCentral South University · CNTongji University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81872823National Natural Science Foundation of China (National Science Foundation of China) 82073782National Natural Science Foundation of China (National Science Foundation of China) 82241002
6 · The paper itself

Abstract

Combining existing drug therapy is essential in developing new therapeutic agents in disease prevention and treatment. In preclinical investigations, combined effect of certain known drugs has been well established in treating extensive human diseases. Attributed to synergistic effects by targeting various disease pathways and advantages, such as reduced administration dose, decreased toxicity, and alleviated drug resistance, combinatorial treatment is now being pursued by delivering therapeutic agents to combat major clinical illnesses, such as cancer, atherosclerosis, pulmonary hypertension, myocarditis, rheumatoid arthritis, inflammatory bowel disease, metabolic disorders and neurodegenerative diseases. Combinatorial therapy involves combining or co-delivering two or more drugs for treating a specific disease. Nanoparticle (NP)-mediated drug delivery systems, i.e., liposomal NPs, polymeric NPs and nanocrystals, are of great interest in combinatorial therapy for a wide range of disorders due to targeted drug delivery, extended drug release, and higher drug stability to avoid rapid clearance at infected areas. This review summarizes various targets of diseases, preclinical or clinically approved drug combinations and the development of multifunctional NPs for combining therapy and emphasizes combinatorial therapeutic strategies based on drug delivery for treating severe clinical diseases. Ultimately, we discuss the challenging of developing NP-codelivery and translation and provide potential approaches to address the limitations. This review offers a comprehensive overview for recent cutting-edge and challenging in developing NP-mediated combination therapy for human diseases.

Indexed as

Multifunctional NanoparticlesNanoparticlesNeoplasmsCombined Modality TherapyDrug Delivery SystemsHumans

Identifiers

PMID38161204
PMCPMC10758001
OpenAlexW4390475387

What Socratic 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 Socratic graph.