Solubility Criteria for Veterinary Drugs

نویسندگان

  • Mike Apley
  • Bryan Crist
  • Mario A. Gonzalez
  • Robert P. Hunter
  • Marilyn N. Martinez
  • Sanja Modric
  • Mark G. Papich
  • Alan F. Parr
  • Jim E. Riviere
  • Margareth R.C. Marques
چکیده

This Stimuli article is the first step toward the development of a general chapter addressing solubility criteria for veterinary drug products. The current criteria for classifying drug solubility are based on human gastrointestinal (GI) physiology. These criteria may not be appropriate to the unique conditions encountered within the GI tract of veterinary species. Thus, this article discusses the relationship between the species-specific GI characteristics and the criteria appropriate for describing drug solubility in veterinary species. Initially the discussion focuses on dogs and cattle, the most common veterinary patients in smalland food-animal practices, respectively. Later the discussion will include various other veterinary species of interest. dx.doi.org/10.14227/DT240117P22 e-mail: [email protected]. *Correspondence should be addressed to: Margareth R. C. Marques, Ph.D., Senior Scientific Liaison, USP, 12601 Twinbrook Parkway, Rockville, MD 20852-1790; tel 301 816 8106, e-mail: [email protected]. Disclaimer: This document represents a consensus of the personal views of the authors and does not necessarily represent the views of the authors' respective companies or organizations, nor does it represent the policies or guidelines of those companies or organizations.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Potential and problems of developing transdermal patches for veterinary applications.

A new frontier in the administration of therapeutic drugs to veterinary species is transdermal drug delivery. The primary challenge in developing these systems is rooted in the wide differences in skin structure and function seen in species ranging from cats to cows. The efficacy of a transdermal system is primarily dependent upon the barrier properties of the targeted species skin, as well as ...

متن کامل

In silico screening of dicarboxylic acids for cocrystallization with phenylpiperazine derivatives based on both cocrystallization propensity and solubility advantage

In silico screening was performed to search for binary solids in which a phenylpiperazine-derivative drug was cocrystallized with a dicarboxylic acid. The phenylpiperazine derivative could be any of 61 such drugs, while the dicarboxylic acid could be any of nine such acids. The uniqueness of this approach was that two criteria had to be fulfilled simultaneously, namely a high propensity for coc...

متن کامل

Recent advances in nanoformulations for co-delivery of curcumin and chemotherapeutic drugs

The application of chemotherapy in cancer treatment has been limited due to cause side effects such as toxicity against normal cells and drug resistance. In recent years, numerous studies have been focused on using natural products with chemotherapeutic drugs to enhance therapeutic efficiency and reduce cytotoxicity. On the other hand, encapsulation of drugs into nanoparticles (NPs) can improve...

متن کامل

Solubility Prediction of Drugs in Supercritical Carbon Dioxide Using Artificial Neural Network

The descriptors computed by HyperChem® software were employed to represent the solubility of 40 drug molecules in supercritical carbon dioxide using an artificial neural network with the architecture of 15-4-1. The accuracy of the proposed method was evaluated by computing average of absolute error (AE) of calculated and experimental logarithm of solubilities. The AE (±SD) of data sets was 0.4 ...

متن کامل

A simple QSPR model to predict aqueous solubility of drugs

Aqueous solubility of a drug/drug candidate is essential data in drug discovery, and an in silico method for predicting the aqueous solubility of drug candidates provides a valuable tool to speed up the process of drug discovery and development. This paper describes a simple quantitative structure property relationship (QSPR) model for predicting the aqueous solubility of drugs which is validat...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2017