| 1 |
Author(s):
Dr. Rohit Baban Chavhan.
Page No : 1-7
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Review article on Effective Patient Counselling & Role of Pharmacist
Abstract
The practise of pharmacy and the idea of pharmacological treatment are both rapidly changing all around the world. Additionally, because of his technical and professional understanding, the pharmacist's role in advocating rational and cautious use of medicine is becoming more crucial. It is well established that patients who are knowledgeable about their drugs and how to take them obtain safe and effective treatment, effective medical care. In addition to the many technical tasks carried out behind the counter, therapeutic pharmacists frequently meet with patients and help with clinical therapies. Giving the patient or their representative a medicine kit alone is insufficient; also, the right medication must be given to the right person with the right information.
Helping a client see everything clearly, possibly from a different perspective. To achieve good change and build a trustworthy relationship, the client may benefit from focusing on feelings, experiences, or behaviour. Effective counselling requires confidentiality.
Keywords: Patient counseling, Attitude and behavior, Privacy and confidentiality, Counseling aids
| 2 |
Author(s):
Ms. Reshma R. Patil, Mr. Kaustubh S. Pishorkar.
Page No : 8-10
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REVIEW OF PREFORMULATION STUDIES FOR NOANOPARTICLE DOSAGE FORMS
Abstract
Preformulation studies are a critical step in the
development of any new drug product. They
provide essential information on the
physicochemical properties of the drug
substance and can help to optimize the
formulation and manufacturing process.
Nanoparticles come in a variety of shapes and
sizes, each with their own unique properties.
We'll explore some common techniques used to
characterize nanosized particles and how they
can be used to assess each formulation's safety
and stability. There are a number of different
factors that can affect preformulation studies of
nanoparticles. Size, surface properties and
chemical composition are some of the most
important factors to consider when formulating
nanoparticles for drug formulation. The results
of these studies can be used to identify potential
problems and guide further research and
development efforts.
| 3 |
Author(s):
Mrs. Dipali M. Kulkarni, Ms. Renuka B. Dhakne.
Page No : 11-13
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REVIEW ON PROCESS ANALYTICAL TECHNOLOGIES FOR TABLET GRANULATION PROCESS
Abstract
The advancement of process analytical
technologies (PAT) has revolutionized the
pharmaceutical industry by providing faster,
more accurate and cost-effective methods for
analyzing drug quality. One particular
application that has greatly benefited from PAT
is tablet granulation processes, which are used
to create tablets with uniform size and shape.
Online PAT refers to the real-time monitoring
of process parameters and quality attributes
during granulation. It helps to optimize the
process by reducing variability and improving
product quality. The use of process analytical
technologies (PAT) in the tablet granulation
process can help to optimize and control the
process, ensuring consistent quality of the final
product. There are some drawbacks to using
PAT, such as the need for specialized
knowledge and skills and high initial
investment costs. With further advances in this
field, it is expected that PAT will become
increasingly utilized by pharmaceutical
companies worldwide.
| 4 |
Author(s):
Dr. A. S. Narute, Ms. Yogita R. Shirsath.
Page No : 14-16
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REVIEW ON IVIVC AND BIOEQUIVALENCE INDICATING DISSOLUTION SPECIFICATIONS
Abstract
The In Vitro In Vivo Correlation (IVIVC)
method is a useful tool for forecasting
bioequivalence between multiple
pharmaceutical dosage forms. The concept
behind IVIVC is that the in vitro release profile
of a drug from dosage form correlates with its
in-vivo performance. It is the process of
determining whether two or more formulations
of the same drug have similar therapeutic
effects. The in vitro-in vivo correlation
(IVIVC) is a predictive calculation of
relationship between the in vitro release of a
drug from a dosage form and its in vivo
performance. IVIVC can be applied as a tool to
help with the development of dissolution
specifications for bioequivalence studies. The
US FDA defines bioequivalent as the extent to
which two products produce the same
pharmacologic effect when administered to
humans. The IVIVC can be applied to help
determine appropriate dissolution
specifications for new drug products. In vitroin vivo correlation (IVIVC) is an important tool
in the development and regulation of drug
products. The goal of IVIVC is to provide a link
between the laboratory results and the
performance of a drug product in humans. This
can help forecast how changes in formulation
or manufacturing processes may affect the
product's performance.
| 5 |
Author(s):
Ms. Renuka B. Dhakne, Dr. Rohit B. Chavhan.
Page No : 17-19
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REVIEW ON QUANTITATIVE THIN LAYER CHROMATOGRAPHY FOR PHYTOPHARMACEUTICALS
Abstract
Phytopharmaceuticals are derived from plants,
and they've been used in medicine for centuries.
There are many different methods of testing the
quality and efficacy of these products.
Quantitative thin layer chromatography
(QTLC) is a powerful analytical tool that can
be used to determine the amount of a particular
compound in a sample. Phytopharmaceuticals
are a natural product that has been extracted
from plants and used for medicinal purposes.
Quantitative TLC can be used to accurately
quantify the levels of these compounds in order
to ensure safety and efficacy. The technique
involves applying a known amount of sample
to a TLC plate and then developing the plate
using an appropriate solvent system
