Anan Suparman
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Pengaruh Lembap, Termal dan Mekanik Pada Proses Manufaktur Sediaan Tablet Muhamad Rizqy Maulana; Fitrianti Darusman; Anan Suparman
Bandung Conference Series: Pharmacy Vol. 3 No. 2 (2023): Bandung Conference Series: Pharmacy
Publisher : UNISBA Press

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Abstract

Quality of pharmaceutical solid preparations is influenced by the selection of solid phases of both active pharmaceutical ingredients (APIs) and additives, formulation design, and manufacturing processes. The pharmaceutical manufacturing process generally involves humid, thermal and mechanical factors. These three things can cause the transformation of the solid form of a BAF. This will certainly affect the stability and bioavailability of the APIs. In the manufacturing process of felt tablet preparations, there are 3 manufacturing methods, namely wet granulation, dry granulation, and direct felt methods. In this research, a literature study was conducted regarding the influence of moisture, thermal and mechanical on the manufacturing process of felt tablet preparations. The results obtained are that the influence of damp, thermal and mechanical in the manufacturing process of pharmaceutical preparations, especially tablet preparations, can result in a phase transformation of APIs solids which will affect the stability and bioavailability of the drug. Kualitas sediaan padat farmasi dipengaruhi oleh pemilihan bahan aktif farmasi (BAF) maupun bahan tambahan, formulasi, dan proses manufaktur. Proses manufaktur sediaan farmasi umumnya melibatkan faktor lembab, termal dan mekanik. Faktor-faktor tersebut dapat menyebabkan transformasi bentuk padatan suatu BAF yang akan mempengaruhi stabilitas dan bioavailabilitas BAF. Pada proses manufaktur sediaan tablet kempa, terdapat 3 metode pembuatan, yaitu metode granulasi basah, granulasi kering, dan kempa langsung. Pada penelitian ini dilakukan study literatur mengenai pengaruh lembap, termal dan mekanik pada proses manufaktur sediaan tablet kempa. Hasil yang didapat yaitu pengaruh lembap, termal dan mekanik pada proses manufaktur sediaan farmasi terutama sediaan tablet dapat mengakibatkan terjadinya transformasi fasa padatan BAF yang akan mempengaruhi stabilitas dan bioavabilitas obat.
Kajian Formulasi Sediaan Floating Drug Delivery System (FDDS) Pada Pengobatan Infeksi Helicobacter pylori Siti Anggina Ismiyati Solihat; Sani Ega Priani; Anan Suparman
Bandung Conference Series: Pharmacy Vol. 3 No. 2 (2023): Bandung Conference Series: Pharmacy
Publisher : UNISBA Press

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.29313/bcsp.v3i2.8890

Abstract

Abstract. Floating drug delivery system (FDDS) is a drug delivery system that can increase the residence time in the stomach. This delivery system was developed to increase the effectiveness of treatment of H. pylori infection, by extending the contact time with the mucosa (target), through the mechanism of floating in gastric fluid. This study aims to assess the formulation of FDDS preparations for the treatment of H. pylori infection. In this study, a systematic literature review was conducted from reputable articles based on inclusion and exclusion criteria. From this study, several conclusions were obtained that FDDS preparations have been developed on the active substances amoxycillin, clarithromycin, ciprofloxacin, metronidazole, and levofloxacin. Formulations using effervescent and non-effervescent systems meet the requirements of a good FDDS preparation, which has a floating lag time of <60-600 seconds and a floating time of >12 hours. The most widely used polymers were sodium alginate and HPMC. Abstrak. Floating drug delivery system (FDDS) merupakan sistem penghantaran obat yang dapat meningkatkan waktu tinggal di lambung. Sistem penghantaran ini dikembangkan untuk meningkatkan efektivitas pengobatan infeksi H. pylori, dengan cara memperpanjang waktu kontak dengan mukosa (target kerja), melalui mekanisme mengapung di cairan lambung. Penelitian ini bertujuan untuk melakukan pengkajian mengenai formulasi pada sediaan FDDS untuk pengobatan infeksi H. pylori. Dalam penelitian ini dilakukan systematic literatur review yang bersumber dari artikel bereputasi berdasarkan kriteria inklusi dan eksklusi. Dari penelitian ini didapatkan beberapa kesimpulan bahwa sediaan FDDS telah dikembangkan pada zat aktif amoxycillin, claritromycin, ciprofloxacin, metronidazol, dan levofloxacin. Formulasi dengan menggunakan sistem effervescent dan non-effervescent memenuhi persyaratan sediaan FDDS yang baik, yaitu memiliki floating lag time <60-600 detik dan floating time >12 jam. Polimer yang paling banyak digunakan adalah sodium alginat dan HPMC.