Process analytical technology tools for monitoring pharmaceutical unit operations: a control strategy for continuous process verification

EJ Kim, JH Kim, MS Kim, SH Jeong, DH Choi - Pharmaceutics, 2021 - mdpi.com
Various frameworks and methods, such as quality by design (QbD), real time release test
(RTRT), and continuous process verification (CPV), have been introduced to improve drug …

Immune cell–camouflaged surface-engineered nanotherapeutics for cancer management

N Jain, S Shahrukh, P Famta, S Shah, G Vambhurkar… - Acta Biomaterialia, 2023 - Elsevier
Nanocarriers (NCs) have shown potential in delivering hydrophobic cytotoxic drugs and
tumor-specific targeting. However, the inability to penetrate the tumor microenvironment and …

Quality by Design (QbD) application for the pharmaceutical development process

SH Lee, JK Kim, JP Jee, DJ Jang, YJ Park… - Journal of …, 2022 - Springer
Abstract Background Quality by Design (QbD) is a pharmaceutical quality management
system that predicts, controls, and systematically responds to risks that may occur in the …

Compartmental approach for modelling twin-screw granulation using population balances

HY Ismail, S Shirazian, M Singh, D Whitaker… - International journal of …, 2020 - Elsevier
In this study, a compartmental population balance model (CPBM) is developed as a
predictive tool of particle size distribution (PSD) for wet granulation in co-rotating twin-screw …

Comparison of modeling methods for DoE‐based holistic upstream process characterization

B Bayer, M von Stosch, G Striedner… - Biotechnology …, 2020 - Wiley Online Library
Upstream bioprocess characterization and optimization are time and resource‐intensive
tasks. Regularly in the biopharmaceutical industry, statistical design of experiments (DoE) in …

Quality by design paradigm for optimization of green stability indicating HPLC method for concomitant determination of fluorescein and benoxinate

AH Kamal, AA Habib, SF Hammad, SM Megahed - Scientific Reports, 2023 - nature.com
A green, robust and fast stability indicating chromatographic method has been developed for
concomitant analysis of fluorescein sodium and benoxinate hydrochloride in the presence of …

Nasal route for antibiotics delivery: Advances, challenges and future opportunities applying the quality by design concepts

SA Mardikasari, B Sipos, I Csóka, G Katona - Journal of Drug Delivery …, 2022 - Elsevier
Proper antibiotic use becomes a fundamental consideration to minimize the chance of
resistance threat. The nasal route has the potential as an appropriate way of administration …

Critical review on the role of excipient properties in pharmaceutical powder-to-tablet continuous manufacturing

PHM Janssen, S Fathollahi, BHJ Dickhoff… - Expert Opinion on …, 2024 - Taylor & Francis
Introduction The pharmaceutical industry is gradually changing batch-wise manufacturing
processes to continuous manufacturing processes, due to the advantages it has to offer. The …

Double-loaded liposomes encapsulating lycopene β-cyclodextrin complexes: Preparation, optimization, and evaluation

S Jhan, AM Pethe - Journal of liposome research, 2020 - Taylor & Francis
In the present investigation, we attempted to develop a lycopene-in-β-CD-in-phospholipid
vesicles (LCPV) with the sole aim of combining the solubilizing power of β-CD with the …

A quality by design approach to optimization of emulsions for electrospinning using factorial and D-optimal designs

MA Badawi, LK El-Khordagui - European journal of pharmaceutical …, 2014 - Elsevier
Emulsion electrospinning is a multifactorial process used to generate nanofibers loaded with
hydrophilic drugs or macromolecules for diverse biomedical applications. Emulsion …