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All Journal Jurnal An-Najat: Jurnal Ilmu Farmasi dan Kesehatan Jurnal Riset Ilmu Kesehatan Umum dan Farmasi Inovasi Kesehatan Global Obat: Jurnal Riset Ilmu Farmasi dan Kesehatan
M. Fithrul Mubarak
Unknown Affiliation
Dentistry Health Professions Medicine & Pharmacology Nursing Public Health Veterinary

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Artikel Review : Evaluasi pada Sediaan Steril Safanda Tiara Fitri; Maulidiyah Cholifah; Isna Wulan Mukarromah; Renny Angreyni; Ferdiana Putri Gita Veronika; Dewi Rahmawati; Dzakiya Zhihrotulwida; M. Fithrul Mubarak
An-Najat Vol. 3 No. 1 (2025): An-Najat: Jurnal Ilmu Farmasi dan Kesehatan
Publisher : STIKes Ibnu Sina Ajibarang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.59841/an-najat.v3i1.2279

Abstract

Sterile preparations are pharmaceutical products that must be free from microorganisms and foreign particles, so they are very important to use in applications that involve direct contact with human body tissue or the circulatory system. The aim of this research is to understand the evaluations that exist on sterile preparations, as well as understanding all the tests carried out on sterile preparations. The method used is the article review method, which sorts thousands of journals into hundreds, tens and up to 5 journals that match the theme. The results obtained are evaluations in sterile preparations, namely organoleptic tests, pH tests, clarity tests, transferred volume tests, homogeneity tests, spreadability tests, adhesion tests, viscosity tests, etc.
Review Artikel : Sediaan Steril Injeksi Miya Hartini Nur Wakhid; Fina Nikmatul W; Windi Tri Wahyuni; Rizki Amalia Putri; Dewi Nur Halisa; Magdalena Kasih Belaon Lebuan; Dewi Rahmawati; Dzakiya Zhihrotulwida; M. Fithrul Mubarak
Jurnal Riset Ilmu Kesehatan Umum dan Farmasi (JRIKUF) Vol. 3 No. 1 (2025): Januari : Jurnal Riset Ilmu Kesehatan Umum dan Farmasi (JRIKUF)
Publisher : LPPM STIKES KESETIAKAWANAN SOSIAL INDONESIA

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.57213/jrikuf.v3i1.506

Abstract

Sterile injection preparations are liquid pharmaceutical preparations that are specifically designed to be administered directly into the body through injection using a sterile syringe or clean injection device. The main requirement for sterile injection preparations is that they must be free from microorganisms, foreign particles, and pyrogenic substances that can trigger fever or infection reactions in patients. Testing the quality of sterile injection preparations includes various aspects, ranging from sterility testing, pyrogenicity testing, clarity testing, to stability testing during the shelf life. Stability testing aims to ensure that the preparation remains safe, effective, and stable until its expiration date. The purpose of this study was to determine the evaluation of sterile injection preparations. The method used is by reviewing journals from Google Scholar, Pubmed, etc. from 2018-2024.  
Artikel Riview: Pengaruh Penggunaan Matriks Pada Tablet Lepas Lambat Maulina Apriani; Dian Ayu Oktavia; Isnaini Sukmaning M; Dila Alvia Rahmasari; Zahwa Natasya Novita P; Alvito Syawal Z; Dewi Rahmawati; Dzakiya Zhihrotulwida; Yani Ambari; M. Fithrul Mubarak
Inovasi Kesehatan Global Vol. 2 No. 2 (2025): Mei : Inovasi Kesehatan Global
Publisher : Lembaga Pengembangan Kinerja Dosen

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.62383/ikg.v2i2.1580

Abstract

Sustained-release tablets are pharmaceutical preparations designed to gradually release the active substance over a specific period, thereby maintaining a constant concentration of the drug in the circulatory system and enhancing therapeutic effectiveness.The development of sustained-release tablets aims to extend the duration of drug action, reduce the frequency of dose administration, and minimize fluctuations in drug levels in the plasma, which ultimately enhances patient compliance and treatment effectiveness, especially in chronic diseases.The purpose of this review is to identify various formulation methods and innovations in the production of sustained-release tablets, as well as to examine the factors that influence the success of these formulations.The method used in this study is a literature review that collects data from various scientific publications over the past five years through online platforms such as Google Scholar, using keywords related to matrix sustained-release tablets and pharmaceutical formulations.The results of the review indicate that various techniques, such as formulating polymer matrices, coating, and encapsulation, have been applied with varying degrees of success depending on the type of active ingredients and excipients used. Some formulation innovations, such as the use of natural polymer matrices and matrix modifications, have proven effective in achieving controlled, stable, and quality-standard-compliant drug release.
Review Artikel: Analisis Formulasi dan Evaluasi Tablet Effervescent Dewi Rahmawati; Dzakiya Zhihrotulwida; M. Fithrul Mubarak; Yani Ambari; Allyssia Salma; Siti Nur Rohmania; Siti Khoiriyah; Achmad Saichoni Arthaganda; Winda Wulandari; Salsabila Firdausi Hernila Putri; Silfi Maslicha
OBAT: Jurnal Riset Ilmu Farmasi dan Kesehatan Vol. 3 No. 3 (2025): May: OBAT: Jurnal Riset Ilmu Farmasi dan Kesehatan
Publisher : Asosiasi Riset Ilmu Kesehatan Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.61132/obat.v3i3.1404

Abstract

The purpose of writing this review article is to analyze the formulation and evaluation of the use of various additives in effervescent tablets. The method used is a literature review taken from journals and other relevant research results regarding the formulation and evaluation of additives in various types of effervescent tablets. The purpose of this analysis is to provide a summary of relevant publications and to improve current understanding in this field. The importance of the formulation and evaluation of additives in effervescent tablets cannot be ignored, because it is a crucial aspect in product development. Decisions in the use of additives must consider the objectives to be achieved, the desired physical characteristics, product stability, and the level of consumer acceptance. With a deep understanding of this formulation and evaluation, we have the potential to produce high-quality effervescent tablets. Variations in additives can also provide different taste and texture characteristics, which of course can affect consumer acceptance.  
Co-Authors Achmad Saichoni Arthaganda Allyssia Salma Alvito Syawal Z Dewi Nur Halisa DEWI RAHMAWATI Dian Ayu Oktavia Dila Alvia Rahmasari Dzakiya Zhihrotulwida Ferdiana Putri Gita Veronika Fina Nikmatul W Isna Wulan Mukarromah Isnaini Sukmaning M Magdalena Kasih Belaon Lebuan Maulidiyah Cholifah Maulina Apriani Miya Hartini Nur Wakhid Renny Angreyni Rizki Amalia Putri Safanda Tiara Fitri Salsabila Firdausi Hernila Putri Silfi Maslicha Siti Khoiriyah Siti Nur Rohmania Winda Wulandari Windi Tri Wahyuni Yani Ambari Zahwa Natasya Novita P