Dergiler / International Journal of PharmATA / 2026 / Volume: 3 Issue: 2

Evaluation Excipients and pH Effects on Impurity of Desloratadine Syrup Formulation

Sayfa
35–40
Yayın Tarihi
2023-05-27
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Both of them were determined to the best formulations about impurity and pH of desloratadine.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:The goal of the research work was to compare the excipient and pH effect develop a stabile pharmaceutical product which is Desloratadine syrup.
📊
Temel Bulgular & Veri:To improve the stability of Desloratadine formulations (F1-F7) were evaluated with different excipients and pH during stability period.
💡
Sonuç & Katkı:Both of them were determined to the best formulations about impurity and pH of desloratadine.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Drug formulation · Desloratadine · syrup

Abstract

The goal of the research work was to compare the excipient and pH effect develop a stabile pharmaceutical product which is Desloratadine syrup. A total of seven formulations were prepared and syrup to stability study. This study is used different excipients and is tried pH for improve product. To improve the stability of Desloratadine formulations (F1-F7) were evaluated with different excipients and pH during stability period. Stability studies were performed to evaluate impurity and assay of desloratine. The rate of initial and 6th months impurity results were compared to F1-F7 formulations. As a result of initial, 3rd and 6th months impurity analysis for F7 formulations were found to be within in limit. According to the evaluation results, the F-7 formulation was chosen as the stabilize and best formulation. Those results showed that the F-7 formulation was stable in the stability studies. Both of them were determined to the best formulations about impurity and pH of desloratadine.

🔖

Bu Makaleye Atıf Yap

Ünal, O. (2023). Evaluation Excipients and pH Effects on Impurity of Desloratadine Syrup Formulation. International Journal of PharmATA, Volume: 3 Issue: 2, 35–40. https://doi.org/10.5152/Pharmata.2023.1179172

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (12)

  1. https://www.researchgate.net/publication/298649069_Formulation_development_and_evaluation_of_desloratadine_tabletsDrug Bank showing Desloratidine (DB00967)
  2. https://sphinxsai.com/july-sept_2010_vol2.3/pharmtech/pharmtechvol2.3july-sept210/PT=70%20(2101-2106).pdf
  3. Raymond C.R, Paul J.S and Sian C.O, Pharmaceutical Excipients, 255-256.
  4. https://patents.google.com/patent/CN101390860A/en
  5. https://patents.google.com/patent/CN104784110A/en
  6. ICH Guideline, “Validation of analytical procedures: text and methodology,” in Proceedings of International Conference on Harmonization, Topic Q2 (R1), Geneva, Switzerland.
  7. https://www.ema.europa.eu/en/documents/variation-report/aerius-h-c-313-x-0033-epar- assessment-report-extension_en.pdf
  8. Development and validation of a novel revesed phase high performance liquid cromatograpy with refractive index detector method for assay of polyvinyl alcohol in an ophthalmic solution.current pharmaceutical analysis 2020
  9. Raymond C.R, Paul J.S and Sian C.O, Pharmaceutical Excipients, 301-303.
  10. Raymond C.R, Paul J.S and Sian C.O, Pharmaceutical Excipients, 185-187.
  11. https://pubchem.ncbi.nlm.nih.gov/compound/Desloratadine
  12. https://go.gale.com/ps/i.do?id=GALE%7CA252944814&sid=googleScholar&v=2.1&it=r&linkaccess=abs&issn=19950772&p=AONE&sw=w&userGroupName=anon%7E6be0a7bb