Evidence map›Paper›PMID 21514661›Full record

ArticleBiomaterials2011

The optimization of polymalic acid peptide copolymers for endosomolytic drug delivery.

Hui Ding, Jose Portilla-Arias, Rameshwar Patil, Keith L Black, Julia Y Ljubimova, Eggehard Holler

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Biomaterials, 2011. 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
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Polymalic acid for translational nanomedicine.Journal of nanobiotechnology · 2022
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Polymer nanomedicines.Advanced drug delivery reviews · 2020
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Polymalic acid nanobioconjugate for simultaneous immunostimulation and inhibition of tumor growth in HER2/neu-positive breast cancer.Journal of controlled release : official journal of the Controlled Release Society · 2013
    Article
  19. Nanotechnology in corneal neovascularization therapy--a review.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2013
    Review
  20. 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

6 authors at 2 institutions in 2 countries.

Hui DingDepartment of Neurosurgery, Cedars-Sinai Medical Center, 110 N. George Burns Rd, Davis 2094A, Los Angeles, CA 90048, USA. Hui.Ding@cshs.org
Jose Portilla-Arias
Rameshwar Patil
Keith L Black
Julia Y Ljubimova
Eggehard Holler
Cedars-Sinai Medical Center · USUniversity of Regensburg · DE

Funding

Novel Nanopolymers to Inhibit Angiogenesis and Increase the Anti-tumor ImmunityR01CA136841 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LJUBIMOVA, JULIA Y, PENICHET, MANUEL L · 2010 to 2014
$2.7M
Nanoconjugate based on polymalic acid for brain tumor treatmentU01CA151815 · NCI · CEDARS-SINAI MEDICAL CENTER · PI LJUBIMOVA, JULIA Y · 2010 to 2014
$2.7M
Tumor drug delivery systems based on polymalic acidR01CA123495 · NCI · CEDARS-SINAI MEDICAL CENTER · PI LJUBIMOVA, JULIA Y · 2006 to 2010
$1.4M
NCI NIH HHS R01 CA123495NCI NIH HHS R01 CA 136841NCI NIH HHS R01 CA136841NCI NIH HHS U01 CA151815
6 · The paper itself

Abstract

Membranolytic macromolecules are promising vehicles for cytoplasmic drug delivery, but their efficiency and safety remains primary concerns. To address those concerns, membranolytic properties of various poly(β-L-malic acid) (PMLA) copolymers were extensively investigated as a function of concentration and pH. PMLA, a naturally occurring biodegradable polymer, acquires membranolytic activities after substitution of pendent carboxylates with hydrophobic amino acid derivatives. Ruled by hydrophobization and charge neutralization, membranolysis of PMLA copolymers increased as a function of polymer molecular weight and demonstrated a maximum with 50% substitution of carboxylates. Charge neutralization was achieved either conditionally by pH-dependent protonation or permanently by masking carboxylates. Membranolysis of PMLA copolymers containing tripeptides of leucine, tryptophan and phenylalanine were pH-dependent in contrast to pH-independent copolymers of Leucine ethyl ester and Leu-Leu-Leu-NH(2) with permanent charge neutralization. PMLA and tripeptides seemed a unique combination for pH-dependent membranolysis. In contrast to nontoxic pH-dependent PMLA copolymers, pH-independent copolymers were found toxic at high concentration, which is ascribed to their nonspecific disruption of plasma membrane at physiological pH. pH-Dependent copolymers were membranolytically active only at acidic pH typical of maturating endosomes, and are thus devoid of cytotoxicity. The PMLA tripeptide copolymers are useful for safe and efficient cytoplasmic delivery routed through endosome.

Indexed as

Drug Delivery SystemsCell MembraneDrug CarriersEndosomesHydrogen-Ion ConcentrationMalatesMolecular StructureMolecular WeightPeptidesPolymersDrug CarriersMalatesPeptidespoly(malic acid)Polymers

Identifiers

PMID21514661
PMCPMC4110056
OpenAlexW1964081042

What OpenQuestion holds

Textmetadata
LicenceTDM
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.