Luthfia Azzahra
Faculty of Pharmacy, Padjadjaran University

Published : 2 Documents Claim Missing Document
Claim Missing Document
Check
Articles

Found 2 Documents
Search

Pharmaceutical Industrial Waste Regulation in Five Countries in Asia Luthfia Azzahra; Nyi Mekar Saptarini
Indonesian Journal of Pharmaceutics Vol 3, Issue 1, Jan - April 2021
Publisher : Universitas Padjadjaran (Unpad)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/idjp.v3i1.33383

Abstract

The pharmaceutical industry produces a various toxic wastes. Generated waste increases the risk of environmental and ecosystem pollution. It is necessary to have proper waste management to prevent waste pollution to the environment. In 1999, WHO published “Guidelines for the Safe Disposal of Unwanted Pharmaceuticals in and after Emergencies”, that contain treatments and safe disposal method, which is appropriate for any country. Many countries had developed and published regulations and guidelines on waste management. This article aimed to review the handling of pharmaceutical industrial waste in five countries in Asia. This review included studies from ProQuest, Crossref, and Google Scholar.  The pharmaceutical industries in Indonesia, India, Japan, Thailand, and China has their own state regulations in order to protect the environment. They also had implemented pharmaceutical industrial waste management following their regulation and guidelines. The method used to treat the waste is similar with WHO guideline. Some factors affecting the country regulations are the insufficient of land and waste management facilities, lack of awareness, low penalties, limited infrastructures, lack of waste testing facilities. The challenge in the future to handle pharmaceutical waste are increasing waste volume, decreasing land for waste management, sewer methods may contaminate water, possible air pollution due to incineration, so it is necessary to have more advanced methods in waste management that are safe for the environment and humans.Keywordz: Industry, Pharmaceutical, Waste Regulation, Asia
Formulation, Characterization, and Herbal Drug Delivery Applications of Ethosome, Transfersome, and Transethosome Luthfia Azzahra; Soraya Ratnawulan Mita; Sriwidodo Sriwidodo
Indonesian Journal of Pharmaceutics Vol 2, Issue 3, Sept - Dec 2020
Publisher : Universitas Padjadjaran (Unpad)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/idjp.v2i3.29154

Abstract

Herbal compounds have different physicochemical properties. Its use on the oral route often has low biological availability. Therefore, alternative transdermal routes are used through the skin. The stratum corneum skin layer is the most difficult layer to penetrate. Therefore it is necessary to use a drug delivery system such as ethosome, transfersome or transethosome to increase transdermal drug delivery. This review article aims to look at the potential of ethosome, transfersome, and transethosome in increasing their ability to deliver herbal drugs in terms of their formulation and characterization. Literature searches were performed using online search engines namely NCBI and Google Scholar with the keywords ‘Transdermal Drug Delivery System’, 'Ethosome', 'Transfersome', and 'Transethosome'. The result showed compositions of ethosomes are phospholipids, water, and ethanol. The composition of transfersome is phospholipid, water, and edge activator. Transethosomes are a combination of phospholipids, water, ethanol, and edge activators. The role of ethanol and edge activator is thought to increase skin permeation. Transdermal drug delivery systems can be used on herbal drugs to increase transdermal drug delivery.Keywords: Transdermal, Ethosome, Transfersome, Transethosome, Herbal.