Evidence map›Paper›PMID 37810010›Full record

ArticleHeliyon2023

Investigation of the treatment potential of Raloxifene-loaded polymeric nanoparticles in osteoporosis: In-vitro and in-vivo analyses.

Zhonghua Guo, Rabia Afza, Muhammad Moneeb Khan, Saif Ullah Khan, Muhammad Waseem Khan, Zakir Ali, Sibgha Batool, Fakhar Ud Din

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. Article
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  9. The Role of Nanomedicine in Benign Gynecologic Disorders.Molecules (Basel, Switzerland) · 2024
    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

8 authors at 3 institutions in 1 country.

Zhonghua GuoDepartment of Orthopaedics, Henan Province Hospital of TCM, Zhengzhou City, Henan Province, 450002, China.
Rabia AfzaDepartment of Botany, Hazara University Mansehra KP, Pakistan.
Muhammad Moneeb KhanDepartment of Pharmacy Quaid-i-Azam University, 45320, Islamabad, Pakistan.
Saif Ullah KhanInstitute of Biotechnology and Microbiology, Bacha Khan University, Charsada, KPK, Pakistan.
Muhammad Waseem KhanInstitute of Pharmaceutical Sciences Khyber Medical University, Peshawar, Pakistan.
Zakir AliDepartment of Pharmacy Quaid-i-Azam University, 45320, Islamabad, Pakistan.
Sibgha BatoolDepartment of Pharmacy Quaid-i-Azam University, 45320, Islamabad, Pakistan.
Fakhar Ud DinDepartment of Pharmacy Quaid-i-Azam University, 45320, Islamabad, Pakistan.
Quaid-i-Azam University · PKBacha Khan University · PKHazara University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis (OP), is a systemic bone disorder associated with low bone mass and bone tissue corrosion. Worsening of the disease condition leads to bone delicacy and fracture. Various drugs are available for the treatment of OP, however they have limitations including poor solubility, bioavailability and toxicity. Herein, Raloxifene-loaded polymeric nanoparticles (RLX-PNPs) were developed and investigated for the treatment of OP with possible solutions to the above mentioned problems. RLX-PNPs were prepared by modified ionic gelation method followed by determining their particle properties. FTIR, DSC and PXRD analysis of the RLX-PNPs were performed to check chemical interaction, thermal behavior and crystallinity, respectively. In-vitro release profile of RLX-PNPs was checked in lab setting, whereas its pharmacokinetics was investigated in Sprague-Dawley rats, in-vivo. Finally, the treatment potential of RLX-PNPs was analyzed in OP induced animal model. The optimized PNPs formulation indicated 134.5 nm particle size, +24.4 mV charge and 91.73% % EE. TEM analysis showed spherical and uniform sized particles with no interactions observed in FTIR analysis. In-vitro release of RLX from RLX-PNPs showed more sustained release behavior as compared to RLX-suspension. Moreover, pharmacokinetic investigations showed a significantly enhanced bioavailability of the RLX-PNPs as well as reduced serum levels of alkaline phosphatase and calcium in OP induced rats when compared with RLX-Suspension after oral administration. Findings of this study suggested that the developed RLX-PNPs have the potential to treat OP due to sustained release and improved bioavailability of the incorporated drug.

Indexed as

BioavailabilityOral administrationOsteoporosisRaloxifene, polymeric nanoparticles

Identifiers

PMID37810010
PMCPMC10559869
OpenAlexW4386629757

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.