Evidence map›Paper›PMID 40627550›Full record

ArticleACS applied bio materials2025

Safe and Efficient Intracellular Release of SN38 via Lysosomal-Responsive SN38-G Loaded Liposomes.

Pierre-Alain Burnouf, Yu-Cheng Su, Shih-Hung Yang

Abstract read
In one paragraph

Article in ACS applied bio materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Pierre-Alain BurnoufInternational Center for Wound Repair and Regeneration, National Cheng-Kung University, Tainan 704, Taiwan.ORCID 0000-0002-6135-1547
Yu-Cheng SuDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 300, Taiwan.
Shih-Hung YangInstitute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.ORCID 0009-0006-6003-9072

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liposomal formulations remain mostly suited for amphiphilic drugs of mild potency. This high selectivity challenges the formulation of potent chemotherapeutics that are preponderantly hydrophobic. Spontaneous accumulation of certain hydrophobic drugs within the lipid bilayer of liposomes leads to aggregation, destabilization, and inadequate drug retention. Here, we depict an alternative approach to load such hydrophobic drugs using SN38, the active form of CPT-11 (Irinotecan, Camptosar), through SN38 glucuronide (SN38-G), its hydrophilic glucuronide prodrug derivative. SN38-G was esterified in acidic methanol or ethanol to produce amphiphilic derivatives SN38-G

Indexed as

Antineoplastic AgentsBiocompatible MaterialsGlucuronidesIrinotecanLiposomesLysosomesCell SurvivalDrug LiberationDrug Screening Assays, AntitumorHumansMaterials TestingMolecular StructureParticle SizeAntineoplastic AgentsBiocompatible MaterialsGlucuronidesIrinotecanLiposomeschemotherapydrug deliveryglucuronideliposomesSN38

Identifiers

PMID40627550
PMCPMC12284848

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.