Evidence map›Paper›PMID 37623112›Full record

ArticleGels (Basel, Switzerland)2023

QbD Design, Formulation, Optimization and Evaluation of Trans-Tympanic Reverse Gelatination Gel of Norfloxacin: Investigating Gene-Gene Interactions to Enhance Therapeutic Efficacy.

Amit Budhori, Abhishek Tiwari, Varsha Tiwari, Ajay Sharma, Manish Kumar, Girendra Gautam, Tarun Virmani, Girish Kumar, Abdulsalam Alhalmi, Omar Mohammed Noman and 2 more

Open access · goldAbstract read
In one paragraph

Article in Gels (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

12 authors at 6 institutions in 3 countries.

Amit BudhoriDevsthali Vidyapeeth Institute of Pharmacy, Lalpur, Rudrapur 263148, India.
Abhishek TiwariPharmacy Academy, IFTM University, Moradabad 244102, India.ORCID 0000-0003-1221-4754
Varsha TiwariPharmacy Academy, IFTM University, Moradabad 244102, India.
Ajay SharmaSchool of Pharmaceutical Sciences, Delhi Pharmaceutical Sciences and Research University, Pushp Vihar, New Delhi 110017, India.ORCID 0000-0002-3623-4445
Manish KumarSchool of Pharmaceutical Sciences, CT University, Ludhiana 142024, India.ORCID 0000-0003-2042-1243
Girendra GautamShri Ram College of Pharmacy, Muzaffarnagar 251001, India.ORCID 0000-0001-9949-6357
Tarun VirmaniSchool of Pharmaceutical Sciences, MVN University, Palwal 121105, India.ORCID 0000-0002-1615-5213
Girish KumarSchool of Pharmaceutical Sciences, MVN University, Palwal 121105, India.ORCID 0000-0002-2917-3277
Abdulsalam AlhalmiDepartment of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi 110062, India.ORCID 0000-0001-7985-4241
Omar Mohammed NomanDepartment of Pharmacognosy, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.ORCID 0000-0003-0902-6381
Sidgi HassonSchool of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool L3 5UG, UK.
Ramzi A MothanaDepartment of Pharmacognosy, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.ORCID 0000-0003-4220-7854
IFTM University · INKing Saud University · SAMVN University · INDelhi Pharmaceutical Science and Research University · INJamia Hamdard · INLiverpool John Moores University · GB

Funding

This research was funded by Researchers Supporting Project number (RSP2023R119), King Saud University, Riyadh, Saudi Arabia RSP2023R119
6 · The paper itself

Abstract

Traditional otic drug delivery methods lack controlled release capabilities, making reverse gelatination gels a promising alternative. Reverse gelatination gels are colloidal systems that transition from a sol to a gel phase at the target site, providing controlled drug release over an extended period. Thermosensitive norfloxacin reverse gelatination gels were developed using a Quality by Design (QbD)-based optimization approach. The formulations were evaluated for their in vitro release profile, rheological behavior, visual appearance, pH, gelling time, and sol-gel transition temperature. The results show that the gelation temperatures of the formulations ranged from 33 to 37 °C, with gelling durations between 35 and 90 s. The drug content in the formulations was uniform, with entrapment efficiency ranging from 55% to 95%. Among the formulations, F10 exhibited the most favorable properties and was selected for a stability study lasting 60 days. Ex-vivo release data demonstrate that the F10 formulation achieved 95.6percentage of drug release at 360 min. This study successfully developed thermosensitive norfloxacin reverse gelatination gels using a QbD-based optimization approach. The selected formulation, F10, exhibited desirable properties in terms of gelling temperature, drug content, and release profile. These gels hold potential for the controlled delivery of norfloxacin in the treatment of ear infections.

Indexed as

controlled drug deliveryear infectionsnorfloxacinQuality by Designreverse gelatination gels

Identifiers

PMID37623112
PMCPMC10454480
OpenAlexW4385840353

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.