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All Journal JURNAL FARMASI GALENIKA Medical Sains : Jurnal Ilmiah Kefarmasian Medical Sains : Jurnal Ilmiah Kefarmasian
Zaelani, Diki
Fakultas Farmasi, Universitas Bhakti Kencana
Health Professions Medicine & Pharmacology

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PENGGUNAAN PATI GANYONG (Canna edulis) SEBAGAI DISINTEGRAN PADA PEMBUATAN TABLET ASAM FOLAT DENGAN METODE CETAK LANGSUNG Azhary, Deny Puriyani; Zaelani, Diki; Lestari, Tri
JURNAL FARMASI GALENIKA Vol 4 No Edisi Khus (2017): Jurnal Farmasi Galenika Volume 4 Edisi Khusus SemNas Tanaman Obat Indon
Publisher : Sekolah Tinggi Farmasi Bandung

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (336.015 KB)

Abstract

Disintegran atau bahan penghancur adalah salah satu komponen penting dalam pembuatan sediaan tablet. Fungsi disintegran adalah memecah tablet sehingga zat aktif dapat dilepaskan. Disintegran yang biasa digunakan dalam formulasi sediaan tablet salah satunya adalah pati. Salah satu tumbuhan penghasil pati adalah ganyong. Ganyong  (Canna edulis) merupakan umbi yang banyak ditemukan di Indonesia dan banyak mengandung pati namun belum banyak digunakan secara optimal. Penelitian ini bertujuan untuk mengetahui bagaimana pengaruh penggunaan pati ganyong (Canna edulis) sebagai disintegran pada tablet asam folat dan dibandingkan dengan disintegran starch 1500. Tablet dibuat dengan metode cetak langsung tanpa proses granulasi. Evaluasi terhadap pati ganyong meliputi kadar air, uji swelling power, kecepatan alir, sudut diam dan kompresibilitas. Sedangkan evaluasi tablet asam folat meliputi keragaman bobot, keseragaman kandungan zat aktif, waktu hancur, disolusi, kekerasan dan friability tablet. Hasil evaluasi menunjukkan pati ganyong memiliki kompresibilitas yang tidak baik (kurang dari 20%). Sedangkan hasil evaluasi tablet menunjukkan tablet yang dibuat dengan pati ganyong memiliki waktu hancur yang sesuai persyaratan tablet yang baik, yaitu kurang dari 15 menit.
REVIEW: PROCESS OF FLUID BED GRANULATOR PARAMETERS AT THE TIME OF SCALE UP IN GRANUL PRODUCTION Diki Zaelani; Yoga Windhu Wardhana; Anis Yohana Chaerunisaa
Medical Sains : Jurnal Ilmiah Kefarmasian Vol 8 No 3 (2023)
Publisher : Sekolah Tinggi Farmasi Muhammadiyah Cirebon

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37874/ms.v8i3.836

Abstract

Scaling up is one of the difficulties faced by the production process of the pharmaceutical industry. We must manufacture in higher quantities than a laboratory size with set requirements as we scale up. Understanding the crucial variables that affect the final product's specifications will aid in choosing appropriate upgrade settings. Fluidized-bed granulation is one of the most frequently used techniques to increase the scale of the pharmaceutical industry. The complex fluidized bed granulation process is influenced by several factors. The most important process variables were the intake air temperature and humidity, concentration of the binder solution, spray rate, atomizing air pressure, and air flow rate. Numerous investigations have examined the effects of large-scale fluid bed granulation. An improved fluid bed granulation technology was employed based on the relative droplet size and moisture content of the powder in the bed after the spraying cycle. These values are comparable, demonstrating that the granulation procedure can be enhanced by considering only the moisture content of the powder and relative droplet size. Keywords: fluid bed granulation, process parameters, scale up
REVIEW: PROCESS OF FLUID BED GRANULATOR PARAMETERS AT THE TIME OF SCALE UP IN GRANUL PRODUCTION Diki Zaelani; Yoga Windhu Wardhana; Anis Yohana Chaerunisaa
Medical Sains : Jurnal Ilmiah Kefarmasian Vol 8 No 3 (2023)
Publisher : Sekolah Tinggi Farmasi Muhammadiyah Cirebon

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37874/ms.v8i3.836

Abstract

Scaling up is one of the difficulties faced by the production process of the pharmaceutical industry. We must manufacture in higher quantities than a laboratory size with set requirements as we scale up. Understanding the crucial variables that affect the final product's specifications will aid in choosing appropriate upgrade settings. Fluidized-bed granulation is one of the most frequently used techniques to increase the scale of the pharmaceutical industry. The complex fluidized bed granulation process is influenced by several factors. The most important process variables were the intake air temperature and humidity, concentration of the binder solution, spray rate, atomizing air pressure, and air flow rate. Numerous investigations have examined the effects of large-scale fluid bed granulation. An improved fluid bed granulation technology was employed based on the relative droplet size and moisture content of the powder in the bed after the spraying cycle. These values are comparable, demonstrating that the granulation procedure can be enhanced by considering only the moisture content of the powder and relative droplet size. Keywords: fluid bed granulation, process parameters, scale up
Co-Authors Afria Hilda Restu Ali Djamhuri Anis Yohana Chaerunisaa Deny Puriyani Azhary Jajang Japar Sodik Reza Pratama Yoga Windhu Wardhana