Evidence map›Paper›PMID 36945256›Full record

ArticleInternational journal of nanomedicine2023

Disulfide Bond-Based SN38 Prodrug Nanoassemblies with High Drug Loading and Reduction-Triggered Drug Release for Pancreatic Cancer Therapy.

Zhi-Xin Zhong, Xu-Zhao Li, Jin-Tao Liu, Nan Qin, Hong-Quan Duan, Xiao-Chuan Duan

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Research Progress of SN38 Drug Delivery System in Cancer Treatment.International journal of nanomedicine · 2024
    Review
  8. Review
  9. Review
  10. Article
  11. 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

6 authors at 1 institution in 1 country.

Zhi-Xin Zhong *School of Pharmacy, Tianjin Medical University, Tianjin, 300070, People's Republic of China.
Xu-Zhao Li *School of Pharmacy, Tianjin Medical University, Tianjin, 300070, People's Republic of China.
Jin-Tao LiuSchool of Pharmacy, Tianjin Medical University, Tianjin, 300070, People's Republic of China.
Nan QinSchool of Pharmacy, Tianjin Medical University, Tianjin, 300070, People's Republic of China.
Hong-Quan DuanSchool of Pharmacy, Tianjin Medical University, Tianjin, 300070, People's Republic of China.
Xiao-Chuan DuanSchool of Pharmacy, Tianjin Medical University, Tianjin, 300070, People's Republic of China.ORCID 0000-0001-5677-8135
Tianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Chemotherapy is a significant and effective therapeutic strategy that is frequently utilized in the treatment of cancer. Small molecular prodrug-based nanoassemblies (SMPDNAs) combine the benefits of both prodrugs and nanomedicine into a single nanoassembly with high drug loading, increased stability, and improved biocompatibility. Methods: In this study, a disulfide bond inserted 7-ethyl-10-hydroxycamptothecin (SN38) prodrug was rationally designed and then used to prepare nanoassemblies (SNSS NAs) that were selectively activated by rich glutathione (GSH) in the tumor site. The characterization of SNSS NAs and the in vitro and in vivo evaluation of their antitumor effect on a pancreatic cancer model were performed. Results: In vitro findings demonstrated that SNSS NAs exhibited GSH-induced SN38 release and cytotoxicity. SNSS NAs have demonstrated a passive targeting effect on tumor tissues, a superior antitumor effect compared to irinotecan (CPT-11), and satisfactory biocompatibility with double dosage treatment. Conclusion: The SNSS NAs developed in this study provide a new method for the preparation of SN38-based nano-delivery systems with improved antitumor effect and biosafety.

Indexed as

NanoparticlesPancreatic NeoplasmsProdrugsCamptothecinCell Line, TumorDisulfidesDrug Delivery SystemsDrug LiberationHumansIrinotecanCamptothecinDisulfidesIrinotecanProdrugs7-ethyl-10-hydroxycamptothecinglutathione responsivenanoassembliespancreatic cancer therapyprodrug

Identifiers

PMID36945256
PMCPMC10024910
OpenAlexW4324373025

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.