PENGARUH LAMANYA PENYIMPANAN TERHADAP MUTU FISIK SEDIAAN SIRUP LORATADINE YANG SUDAH DIBUKA

Main Article Content

indah trilestari

Abstract

ABSTRACT

 


Loratadine is a second-generation group of antihistamine drugs that block H1-receptors. In general, people use a solution of loratadine syrup at the time of allergy only, so the preparations are still left a lot and the public will tend to store the syrup. Drug preparations in the form of a solution or syrup are easily damaged. Research objectives : to determine the effect of the duration of storage of loratadine solution preparations and their significant value that has been opened for 15 days, 30 days and 45 days compared to 0 days as a control then conducted a physical quality test of loratadine solution preparations which includes organoleptic evaluation, pH determination test and level determination test. Research method : ecperimental using UV-Vis Spectrophotometry tool with a maximum wavelength of 247.0 nm. Before determining the value of the level performed lineritas value of y = 0.0308x + 0.0297.


Research result : the results of organoleptic evaluation of loratadine solution preparations with a clear color, distinctive smell, bitter sweetness. Average pH result with 0 days of storage as control


= 4.7 ; 15 days = 4.5 ; 30 days = 4.4 and 45 days = 4.5. And obtained the average yield percentage of the rate with a storage duration of 0 days as a control = 100.70%, 15 days = 101.19%, 30 days


= 95.54%, and 45 days = 91.80%. Then the data of pH parameters and content of levels in the statistical test one way anova with a significant value of 0.000. Conclusion: in this study there are differences in physical quality in the preparation of loratadine syrup to variations in the length of storage after opening, namely in the parameters of pH and content of levels.


 


Keywords: Loratadine, Syrup, Storage Duration, UV-Vis Spectrophotometry, pH, Dosage Content.

Downloads

Download data is not yet available.

Article Details

How to Cite
trilestari, indah. (2022). PENGARUH LAMANYA PENYIMPANAN TERHADAP MUTU FISIK SEDIAAN SIRUP LORATADINE YANG SUDAH DIBUKA. AFAMEDIS, 3(1), 63-75. https://doi.org/10.61609/afamedis.v3i1.52
Section
Articles

References

A.V.Glushchenko, V.A.Georgiyants, N.Yu.Bevz (2014). Development And Evaluation Of Validation Characteristic Of The Quantitative Determination Method For Loratadine In The Syrup. News Of Pharmacy 1(77). Hal 31-35.

Aisyah Fatmawaty, Michrun Nisa, dan Radhia Riski, 2019. Teknologi sediaan farmasi. Yogyakarta.

Andari, 21013. Perbandingan Penetapan Kadar Keteprofen Tablet secara Alkalimetri dengan
Spektrofotometri-Uv. Jurnal Eduhealt 3(2). Hal 114-119.
Anonim, 1995. Farmakope Indonesia. Edisi
IV. Jakarta : Departemen Kesehatan RI.

Ansel. H.C.. 1989. Pengantar Bentuk Sediaan Farmasi, Diterjemahkan Oleh Ibrahim, Asmanizar, Iis Aisyah, Edisi Keempat, 255-271. 607-608. 700. Jakarta, UI Press.

Aremu, O.I., & Oduyela, O.O. (2015). Evaluation of Metronidazole suspensions. African Journal of Pharmacy and Pharmacy and Pharmacology. 9 (12), 439-450.

Arisandi, W, S., 2008. Pengaruh pH Terhadap Stabilitas Sirup Paracetamol, (online) http://www.scribd.com.diakses 07
November 2019).

Carstensen, J.T & C.T Rhodes, 2000. Drug Stability Principles And Practice, Marcel Dekker. Inc, New York, USA.

Connors, K.A., Amidon, G.L. and Stella, V.J., 1986. Chemical Stability of Pharmaceutical. John Willey and Sons, NewYork.

Departemen Kesehatan RI. 1979. Farmakope Indonesia. Edisi III. Jakarta: Depkes RI.

Harmita, 2004. Petunjuk Pelaksanaan Validasi Metode dan Cara Perhitungan, Majalah Ilmu Kefarmasian, Vol.I, No. 3, Desember.

Ikawati, Sullies, 2010. Cerdas Mengamati Obat. Yogyakarta: Bursa Ilmu.
Kementerian Kesehatan RI. 2020. Farmakope Indonesia Edisi VI. Jakarta : Kementerian Kesehatan RI.
Loyd V. Allen Jr, 2015. Bentuk Sediaan Farmasetis Dan System Penghancur Obat. Diterjemahkan oleh Lucia Hendriati Dan Kuncoro Foe.9th ed., Penerbit Buku Kedokteran Egc, Jakarta.

Luawo, dkk, 2012. Penyimpanan Obat.
Surabaya.

Luawo. E.F., Citraningtyas, G., Kojong. N. (2012). Pengaruh Suhu Terhadap Stabilitas Berbagai Produk Tablet Nifedipin. Pharmacon 2 (11). Hal
112-118

Marzuki, Asnah. 2012. Kimia AnalisisFarmasi. Makassar; Dua Satu Press.

McEvory G.K., 2008. AHFS Drug Information, American Society Of Health Sistem, USA. Hal 40-45.

Nayak R.K., Manna K.,(2011). Current Developments In Orally Disintegrating Tablet Technology,
J. Pharm Educ. Res 2(1). Hal 21-34.

Notoatmodjo, S. 2010. Metodologi Penelitian Kesehatan. Jakarta : Rineka Cipta.


Putra, I Gusti N. dkk. 2014. Petunjuk Dan Buku Kerja Praktikum Formulasi Dan Teknologi Sediaan Steril. Universitas Udayana, Bali.

Rohman, A. 2007. Kimia Farmasi Analis: Spektrofotometri UV dan Tampak (visible). Yogyakarta : Pustaka Pelajar.

Vadas, E.B. 2010. Stability Of Pharmaceutical Products. Dalam Remington: The Science and Practice of Pharmacy. Volume 1. Editor Alfonso Gennaro. London: Lippincott Williams & Wilkins. Hal 988-989.

Wunas, Yeanny dan Susanti. 2011. Analisa Kimia Farmasi Kuantitatif (Revisi 2). Makassar; Laboratorium Kimia Farmasi Fakultas Farmasi UNHAS.

Erina S., Samsul A. Y. 2019. Produksi bibit tanaman dengan menggunakan teknik kultur jaringan.