Evidence map›Paper›PMID 39458747›Full record

ArticlePolymers2024

Sublingual Fast-Dissolving Thin Films of Loratadine: Characterization, In Vitro and Ex Vivo Evaluation.

Yahya Alhamhoom, Ashitha Kakarlapudi Said, Avichal Kumar, Shivakumar Hagalavadi Nanjappa, Divya Wali, Mohamed Rahamathulla, Syeda Ayesha Farhana, Mohammed Muqtader Ahmed, Thippeswamy Boreddy Shivanandappa

Abstract read
In one paragraph

Article in Polymers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

9 authors.

Yahya AlhamhoomDepartment of Pharmaceutics, College of Pharmacy, King Khalid University, Al Faraa, Abha 62223, Saudi Arabia.ORCID 0000-0002-8368-9047
Ashitha Kakarlapudi SaidDepartment of Pharmaceutics, KLE College of Pharmacy, Rajajinagar, Bengaluru 560010, India.
Avichal KumarDepartment of Pharmaceutics, KLE College of Pharmacy, Rajajinagar, Bengaluru 560010, India.ORCID 0000-0003-3893-3407
Shivakumar Hagalavadi NanjappaDepartment of Pharmaceutics, KLE College of Pharmacy, Rajajinagar, Bengaluru 560010, India.ORCID 0000-0003-1596-9941
Divya WaliDepartment of Pharmaceutics, KLE College of Pharmacy, Rajajinagar, Bengaluru 560010, India.
Mohamed RahamathullaDepartment of Pharmaceutics, College of Pharmacy, King Khalid University, Al Faraa, Abha 62223, Saudi Arabia.ORCID 0000-0001-8826-3718
Syeda Ayesha FarhanaDepartment of Pharmaceutics, College of Pharmacy, Qassim University, Buraidah 51452, Saudi Arabia.ORCID 0000-0001-8154-7718
Mohammed Muqtader AhmedDepartment of Pharmaceutics, College of Pharmacy, Prince Sattam Bin Abdul Aziz University, Al Kharj 11942, Saudi Arabia.
Thippeswamy Boreddy ShivanandappaDepartment of Biomedical Science, College of Pharmacy, Shaqra University, Al-Dawadmi Campus, Al-Dawadmi 11961, Saudi Arabia.ORCID 0000-0001-9960-2498

Funding

Deanship of scientific Reserach King Khalid University RGP 2 /66/45
6 · The paper itself

Abstract

Loratadine (LOR) is a second-generation antihistamine that exhibits a low and variable oral bioavailability (10-40%) and delayed onset owing to poor solubility and an extensive first-pass effect. Therefore, in light of the clinical need, the main goal of the present study was to develop sublingual fast-dissolving thin films of LOR-citric acid co-amorphous systems (LOR-CAs) with the aim of eliciting a faster onset and improving the bioavailability. We formulated sublingual fast-dissolving thin films of LOR by a film-casting technique using hydrophilic polymers like hydroxypropyl methylcellulose (HPMC E15), polyvinyl pyrrolidone K30 (PVP K30), and hydroxypropyl cellulose EL (HPC-EF) and citric acid as a pH modulator, while glycerin served as a plasticizer. The sublingual fast-dissolving thin films were characterized by FTIR, SEM, DSC, and XRD and evaluated for in vitro dissolution and ex vivo mucoadhesion. The best formulation (F1) developed using HPMC E15 as a polymer, glycerin as a plasticizer, and citric acid as a pH modulator was found to be the optimized formulation as it was smooth, clear, flexible, and displayed good mucoadhesion (11.27 ± 0.418 gm/cm

Indexed as

bioavailabilityhydroxypropyl methylcellulose (E15)in vitro studyloratadine sublingual thin filmmucoadhesionpolyvinyl pyrrolidone (K30)

Identifiers

PMID39458747
PMCPMC11511290

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.