Evidence map›Paper›PMID 29124977›Full record

ReviewDrug delivery2017

Drug delivery for bioactive polysaccharides to improve their drug-like properties and curative efficacy.

Zhe Li, LiNa Wang, Xiao Lin, Lan Shen, Yi Feng

Open access · goldAbstract readReview
In one paragraph

Review in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Frontiers in pharmacology · 2024
    Article
  7. Review
  8. Wild vs. CultivatedPlants (Basel, Switzerland) · 2023
    Article
  9. Article
  10. 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

5 authors at 2 institutions in 2 countries.

Zhe Lia College of Chinese Materia Medica , Shanghai University of Traditional Chinese Medicine , Shanghai , PR China.
LiNa Wanga College of Chinese Materia Medica , Shanghai University of Traditional Chinese Medicine , Shanghai , PR China.
Xiao Lina College of Chinese Materia Medica , Shanghai University of Traditional Chinese Medicine , Shanghai , PR China.
Lan Shena College of Chinese Materia Medica , Shanghai University of Traditional Chinese Medicine , Shanghai , PR China.
Yi Fengb Engineering Research Center of Modern Preparation Technology of TCM of Ministry of Education, Shanghai University of Traditional Chinese Medicine , Shanghai , PR China.
Shanghai University of Traditional Chinese Medicine · CNScleroderma Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over several decades, natural polysaccharides (PSs) have been actively exploited for their wide bioactivities. So far, many PS-related reviews have been published; however, none focused on the delivery of bioactive PSs as therapeutic molecules. Herein, we summarized and discussed general pharmacokinetic properties of PSs and drug delivery systems (DDSs) developed for them, together with the challenges and prospects. Overall, most bioactive PSs suffer from undesirable pharmacokinetic attributes, which negatively affect their efficacy and clinical use. Various DDSs therefore have been being utilized to improve the drug-like properties and curative efficacy of bioactive PSs by means of improving oral absorption, controlling the release, enhancing the in vivo retention ability, targeting the delivery, exerting synergistic effects, and so on. Specifically, nano-sized insoluble DDSs were mainly applied to improve the oral absorption and target delivery of PSs, among which liposome was especially suitable for immunoregulatory and/or anti-ischemic PSs due to its synergistic effects in immunoregulation and biomembrane repair. Chemical conjugation of PSs was mainly utilized to improve their oral absorption and/or prolong their blood residence. With formulation flexibility, in situ forming systems alone or in combination with drug conjugation could be used to achieve day(s)- or month(s)-long sustained delivery of PSs per dosing.

Indexed as

AnimalsDelayed-Action PreparationsDrug Delivery SystemsHumansLiposomesPolysaccharidesDelayed-Action PreparationsLiposomesPolysaccharidesconjugationin situ forming systemnano-sized carrierpharmacokineticsPolysaccharide

Identifiers

PMID29124977
PMCPMC8812577
OpenAlexW2767373360

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.