Evidence map›Paper›PMID 30201818›Full record

ArticleAntimicrobial agents and chemotherapy2018

Novel Self-Assembled Micelles Based on Cholesterol-Modified Antimicrobial Peptide (DP7) for Safe and Effective Systemic Administration in Animal Models of Bacterial Infection.

Rui Zhang, Fengbo Wu, Lei Wu, Yaomei Tian, Bailing Zhou, Xueyan Zhang, Rong Huang, Chaoheng Yu, Gu He, Li Yang

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Review
  2. KK2DP7 Stimulates CD11bAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Advanced delivery systems for peptide antibiotics.Advanced drug delivery reviews · 2023
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Engineering neoantigen vaccines to improve cancer personalized immunotherapy.International journal of biological sciences · 2022
    Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
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.

Rui Zhang *State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China.
Fengbo Wu *State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China.ORCID 0000-0003-0042-8456
Lei WuState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China.
Yaomei TianState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China.
Bailing ZhouState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China.
Xueyan ZhangState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China.
Rong HuangState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China.
Chaoheng YuState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China.
Gu HeState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China hegu@scu.edu.cn yl.tracy73@gmail.com.
Li YangState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Sichuan, China hegu@scu.edu.cn yl.tracy73@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Owing to their broad-spectrum antibacterial properties, multitarget effects, and low drug resistance, antimicrobial peptides (AMPs) have played critical roles in the clinical therapy of drug-resistant bacterial infections. However, the potential hazard of hemolysis following systemic administration has greatly limited their application. Here, we developed a novel AMP derivative, DP7-C, by modifying a formerly identified highly active AMP (DP7) with cholesterol to form an amphiphilic conjugate. The prepared DP7-C easily self-assembled into stable nanomicelles in aqueous solution. The DP7-C micelles showed lower hemolytic activity than their unconjugated counterparts toward human red blood cells and a maximum tolerated dose of 80 mg/kg of body weight in mice via intravenous injection, thus demonstrating improved safety. Moreover, by eliciting specific immunomodulatory activities in immune cells, the DP7-C micelles exerted distinct therapeutic effects in zebrafish and mouse models of infection. In conclusion, DP7-C micelles may be an excellent candidate for the treatment of bacterial infections in the clinic.

Indexed as

AnimalsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesBacterial InfectionsCholesterolDrug Resistance, BacterialFemaleHemolysisHumansMiceMice, Inbred BALB CMice, Inbred C57BLMicellesMicrobial Sensitivity TestsModels, AnimalZebrafishAnti-Bacterial AgentsAntimicrobial Cationic PeptidesCholesterolMicellesantimicrobial peptidehemolytic effectimmune regulationmicellesystemic administration

Identifiers

PMID30201818
PMCPMC6201105

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.