Evidence map›Paper›PMID 29098877›Full record

ArticleDrug delivery2017

Hydrophobic binding peptide-conjugated hybrid lipid-mesoporous silica nanoparticles for effective chemo-photothermal therapy of pancreatic cancer.

Raj Kumar Thapa, Hanh Thuy Nguyen, Milan Gautam, Aarajana Shrestha, Eung Seok Lee, Sae Kwang Ku, Han-Gon Choi, Chul Soon Yong, Jong Oh Kim

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Advances and Prospects in the Treatment of Pancreatic Cancer.International journal of nanomedicine · 2023
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Theranostic nanoparticles for detection and treatment of pancreatic cancer.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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

9 authors at 3 institutions in 1 country.

Raj Kumar Thapaa College of Pharmacy , Yeungnam University , Gyeongsan , Gyeongsanbuk-do , Republic of Korea.
Hanh Thuy Nguyena College of Pharmacy , Yeungnam University , Gyeongsan , Gyeongsanbuk-do , Republic of Korea.
Milan Gautama College of Pharmacy , Yeungnam University , Gyeongsan , Gyeongsanbuk-do , Republic of Korea.
Aarajana Shresthaa College of Pharmacy , Yeungnam University , Gyeongsan , Gyeongsanbuk-do , Republic of Korea.
Eung Seok Leea College of Pharmacy , Yeungnam University , Gyeongsan , Gyeongsanbuk-do , Republic of Korea.
Sae Kwang Kub College of Korean Medicine , Daegu Haany University , Gyeongsan , South Korea.
Han-Gon Choic College of Pharmacy , Hanyang University , Sangnok-gu, Ansan , Republic of Korea.
Chul Soon Yonga College of Pharmacy , Yeungnam University , Gyeongsan , Gyeongsanbuk-do , Republic of Korea.
Jong Oh Kima College of Pharmacy , Yeungnam University , Gyeongsan , Gyeongsanbuk-do , Republic of Korea.
Yeungnam University · KRDaegu Haany University · KRHanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoparticle-based drug delivery systems are designed to reach tumor sites based on their enhanced permeation and retention effects. However, a lack of interaction of these nanoparticles with cancer cells might lead to reduced uptake in the tumors, which might compromise the therapeutic efficacy of the system. Therefore, we developed bortezomib and IR-820-loaded hybrid-lipid mesoporous silica nanoparticles conjugated with the hydrophobic-binding peptide, cyclosporine A (CsA), and referred to them as CLMSN/BIR. Upon reaching the tumor site, CsA interacts hydrophobically with the cancer cell membranes to allow effective uptake of the nanoparticles. Nanoparticles ∼160 nm in size were prepared and the stability of IR-820 significantly improved. High cellular uptake of the nanoparticles was evident with pronounced apoptotic effects in PANC-1 and MIA PaCa-2 cells that were mediated by the chemotherapeutic effect of bortezomib and the photothermal and reactive oxygen species generation effects of IR-820. An in vivo biodistribution study indicated there was high accumulation in the tumor with an enhanced photothermal effect in PANC-1 xenograft mouse tumors. Furthermore, enhanced antitumor effects in PANC-1 xenograft tumors were observed with minimal toxicity induction in the organs of mice. Cumulatively, these results indicated the promising effects of CLMSN/BIR for effective chemo-phototherapy of pancreatic cancers.

Indexed as

AnimalsBortezomibCell Line, TumorCyclosporineDrug Delivery SystemsFemaleHumansHydrophobic and Hydrophilic InteractionsIndocyanine GreenLipidsMiceMice, Inbred BALB CMice, NudeNanoparticlesPancreatic NeoplasmsParticle SizeBortezomibCyclosporineIndocyanine GreenIR 820LipidsPeptidesReactive Oxygen SpeciesSilicon DioxideBortezomibchemo-phototherapyhydrophobic-binding peptideIR-820pancreatic cancer

Identifiers

PMID29098877
PMCPMC8240994
OpenAlexW2766608659

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.