scholarly journals Influence of the octogen quality and production scale on characteristics of granulated plastic bonded explosive

2020 ◽  
Vol 26 (2) ◽  
pp. 183-190
Author(s):  
Hicham Kemmoukhe ◽  
Slavica Terzic ◽  
Mirjana Dimic ◽  
Danica Simic ◽  
Zijah Burzic ◽  
...  

The compositions of granulated plastic bonded explosive (PBX), based on octogen (HMX) and Estane polymer were prepared by aqueous/solvent slurry coating tehnique, on a laboratory and industrial scale. Scale-up was done in an environmentally friendly and cost-effective way: with provided recyclage and reuse of the used organic solvent. The quality of the obtained granulated PBX samples was observed trough the following analyses: the quality of polymer coating layer on HMX crystals was examined by microscopic analysis; the phlegmatizer content in PBX samples was determined; granulometric analysis and the tests of sensitivity to friction and impact were carried out. Compressibility of granulated PBX was determined by pressing. Measured detonation velocities of pressed PBX charges were compared. The obtained properties of the examined pressed PBX indicated that it may find application as a promising main explosive charge in cumulative warheads.

2021 ◽  
Vol 20 ◽  
Author(s):  
Rajib Malla ◽  
Dhaval Shah ◽  
Chinmay Gajendragadkar ◽  
Vijayalakshmi Vamanan ◽  
Deepak Singh ◽  
...  

A perfusion approach at N-1, where cells stay in the exponential growth phase throughout the entire culture duration, is becoming more common as a strategy for process intensification. This is because the higher cell densities it generates allows manufacturers to skip seed stages and reduce process transfer time through multiple bioreactor sizes, thus providing more cost-effective biologics production in smaller facilities. However, this N-1 perfusion approach requires optimization. In this article, we describe the development and proof-of-concept studies with single-use rocking motion perfusion bioreactors in which we have achieved a ten-fold increase in viable cell count in N-1 seed stage, compared to the fed-batch control process, in just 6–8 days. We also mention in detail how we inoculated a 50 L bioreactor production run using this intensified seed train and show comparable growth kinetics and yield with a control process, also at 50 L scale. Using this intensification approach in the future will help our manufacturing facility, the Biopharma Division of Intas Pharmaceuticals Ltd., reach 4000 L production-scale volumes with fewer process transfer steps, and without changing the feeding strategy or production bioreactors of our biologics’ portfolio.


e-xacta ◽  
2018 ◽  
Vol 11 (2) ◽  
pp. 9
Author(s):  
Felipe Eliseu Meireles ◽  
Tayenne Lalesca Moreira Estevam ◽  
Leonardo De Melo Leite

<p><em>O processo de coloração de lâminas hematológicas para análise microscópica é utilizado para que seja possível realizar a contagem das células do sangue. Atualmente existem as formas automática, semiautomática e manual para a realização deste processo. Esse artigo apresenta o desenvolvimento do protótipo de um sistema embarcado para coloração automática de lâminas hematológicas, concebido para torná-lo flexível, confiável e de custo atrativo.  O protótipo desenvolvido foi testado em laboratório comercial seguindo os protocolos de coloração estendida e de colocação rápida. A partir da obtenção de fotos microscópicas das lâminas, certificadas por laboratoristas credenciados, pode-se comprovar a qualidade do resultado da coloração e, consequentemente, a eficiência do protótipo desenvolvido. </em></p><p> </p><p><em>Abstract</em></p><p><em></em><em>The staining hematological slides process for microscopic analysis is used to be possible perform the count of the blood cells. Currently there are the automatic, semi automatic and manual forms for carrying out this process. This article presents the development of the prototype of an embedded system for automatic staining of haematological slides, designed to make it flexible, reliable and cost-effective. The prototype developed was tested in commercial laboratory following the protocols of extended staining and fast staining. By obtaining microscopic photos of the slides, certified by accredited laboratoristas, it is possible to prove the quality of the coloring result and, consequently, the efficiency of the developed prototype.</em></p>


2019 ◽  
Vol 2019 ◽  
pp. 1-14 ◽  
Author(s):  
Hidenori Kawasaki ◽  
Toshinori Shimanouchi ◽  
Yukitaka Kimura

The objective of this review is to survey the development of the optimization of lyophilization. The optimization study of the lyophilizer has been roughly developing by the order of (i) trial-and-error approach, (ii) process modeling using mathematical models, (iii) scalability, and (iv) quality-by-design. From the conventional lyophilization studies based on the trial-and-error, the key parameters to optimize the operation of lyophilization were found out, i.e., critical material attributes (CMAs), critical process parameters (CPPs), and critical quality attributes (CQAs). The mathematical models using the key parameters mentioned above have been constructed from the viewpoints of the heat and mass transfer natures. In many cases, it is revealed that the control of the primary drying stage determines the outcome of the lyophilization of products, as compared with the freezing stage and the secondary drying stage. Thus, the understanding of the lyophilization process has proceeded. For the further improvement of the time and economical cost, the design space is a promising method to give the possible operation range for optimizing the lyophilization operation. This method is to search the optimized condition by reducing the number of key parameters of CMAs, CPPs, and CQAs. Alternatively, the transfer of lyophilization recipe among the lab-, pilot-, and production-scale lyophilizers (scale-up) has been examined. Notably, the scale-up of lyophilization requires the preservation of lyophilization dynamics between the two scales, i.e., the operation of lab- or pilot-scale lyophilizer under HEPA-filtrated airflow condition. The design space determined by focusing on the primary drying stage is large and involves the undesired variations in the quality of final products due to the heterogeneous size distribution of ice crystals. Accordingly, the control of the formation of the ice crystal with large size gave impact on the product quality and the productivity although the large water content in the final product should be improved. Therefore, the lyophilization should take into account the quality by design (QbD). The monitoring method of the quality of the product in lyophilization process is termed the “process analytical technology (PAT).” Recent PAT tools can reveal the lyophilization dynamics to some extent. A combination of PAT tools with a model/scale-up theory is expected to result in the QbD, i.e., a quality/risk management and an in situ optimization of lyophilization operation.


Author(s):  
Egbula N. Eni ◽  
Afiong Oku ◽  
Roseline E. Duke

Aim: To determine the magnitude of presbyopia and the effect of uncorrected presbyopia on vision-related quality of life in Calabar South, Nigeria. Study Design: A community-based, descriptive cross-sectional study. Place and Duration of Study: Calabar South Local Government Area, Nigeria, between November 2016 and February 2017. Methods: We included 422 adults (198 men, 224 women) aged 35 years and above, selected by cluster random sampling. Subjective distance refraction was done on all participants with distant visual acuity less than 6/6. Near visual acuity was assessed at 40 centimetres with a Times Roman near vision (British N system) chart, with distant correction in place if required. Presbyopia was defined as inability to read N8 at 40 centimetres unaided or with habitually worn distance refractive correction, with improvement of near vision by at least one line on a Times Roman near vision chart with use of a plus lens. An adapted and validated quality of life questionnaires were administered to the participants. Results: A total of 422 participants were examined and interviewed. The prevalence of presbyopia was 55.5%. There was no significant association between gender and prevalence of presbyopia. The presbyopia correction coverage in the study population was 38.0% with a strong positive correlation between age and the required near vision spectacle lens power (r = 0.88, p < .001). Another key finding was a significant association between uncorrected presbyopia and reduced quality of life. Conclusion: This study has demonstrated that the burden of presbyopia in the study population is enormous in spite of the fact that it has a cost effective intervention. The key findings in this study underscore the need to scale up presbyopic correction services in the study area.


Author(s):  
John B. Noble

Once a potential indication has been found for a given protein product, it is necessary to produce increasing quantities to satisfy the demands of market trial activities. In the majority of cases, this will lead to scale-up of the purification process to meet demand whilst maintaining the safety, efficacy, and quality of the product. The following chapter provides an overview of the key issues that will arise during scale-up and provides the reader with practical advice on process and equipment selection. The text examines the key issues in defining production scale, identifies critical scale-up and development issues on an overall process basis, presents practical tips on scale-up, and concludes with two industrial scale-up case studies. The final choice of purification scale must reflect the most cost-effective solution for the whole of an organization and as such there are a great many influences to be considered. As a result the development process is an iterative exercise in which the production demand and schedule are balanced against available resources. A step-by-step approach to choice of purification scale is developed below: (a) Step 1: define volume of product required and when it is needed. (b) Step 2: develop a preliminary scale-up schedule. (c) Step 3: match scale and production schedule to production resources. Each of these steps will now be developed further. From preliminary product trials it will be possible to develop a schedule of product demand against time which can be used as the building block for step 2. Typically for pharmaceutical products the schedule will included materials for pre-clinical trials, phases I-III clinical trials, and commercial manufacture. During trials a defined quantity of product will be required over a clearly defined period whilst, once a product has been approved, demand will be less well defined and generally increase gradually over time to market saturation. From the schedule developed in step 1 and a knowledge of the approximate process yields, a preliminary assessment of overall raw material throughput can be developed. This can then be broken down and combined with information on product shelf-life to assess the most appropriate production strategy for each stage of a product’s life.


Author(s):  
Adrienne F.A. Meyers ◽  
Paul Sandstrom ◽  
Thomas N. Denny ◽  
Mackenzie Hurlston ◽  
Terry B. Ball ◽  
...  

In 2015, UNAIDS launched the 90-90-90 targets aimed at increasing the number of peopleinfected with HIV to become aware of their status, access antiretroviral therapies and ultimatelybe virally suppressed. To achieve these goals, countries may need to scale up point-of-care (POC) testing in addition to strengthening central laboratory services. While decentralisingtesting increases patient access to diagnostics, it presents many challenges with regard totraining and assuring the quality of tests and testing. To ensure synergies, the London Schoolof Hygiene & Tropical Medicine held a series of consultations with countries with an interestin quality assurance and their implementing partners, and agreed on an external qualityassessment (EQA) programme to ensure reliable results so that the results lead to the bestpossible care for HIV patients. As a result of the consultations, EQA International wasestablished, bringing together EQA providers and implementers to develop a strategic planfor countries to establish national POC EQA programmes and to estimate the cost of setting upand maintaining the programme. With the dramatic increase in the number of proficiencytesting panels required for thousands of POC testing sites across Africa, it is important tofacilitate technology transfer from global EQA providers to a network of regional EQA centresin Africa for regional proficiency testing panel production. EQA International will continue toidentify robust and cost-effective EQA technologies for quality POC testing, integrating noveltechnologies to support sustainable country-owned EQA programmes in Africa.


2004 ◽  
Vol 5 (2) ◽  
pp. 239-242 ◽  
Author(s):  
P. H. Flore

AbstractIf vaccines are to reliably prevent disease, they must be developed, produced and quality-controlled according to very strict regulations and procedures. Veterinary viral vaccine registrations are governed by different rules in different countries, but these rules all emphasize that the quality of the raw materials—the cells, eggs, animals or plants that are used in production—need to be carefully controlled. The veterinary vaccine business is also very cost-conscious. Emphasis over the last 5–10 years has therefore been to develop culture systems that minimize labor and sterility problems and thus provide for reliable and cost-effective production. Implementing these often more complex systems in a production environment takes considerable effort, first in scale-up trials and further down the line in convincing production personnel to change their familiar system for something new and possibly untried. To complete scale-up trials successfully, it is absolutely necessary to understand the biochemistry of the cells and the influence of the virus on the cells under scale-up and later production conditions. Once a viral product can be produced on a large scale, it is imperative that the quality of the end-product is controlled in an intelligent way. One needs to know whether the end-product performs in the animal as was intended during its conception in the research and development department. The development of the appropriate tests to demonstrate this plays an important role in the successful development of a vaccine.


Author(s):  
I.N. Voronchikhina ◽  
◽  
A.G. Marenkova ◽  
V. S. Rubets ◽  
V. V. Pylnev

The results of elements development of varietal agrotechnics of a new high-potential line 238h of winter triticale presented. It was identified that under the conditions of 2020 the most cost effective fertilizer system is an early spring application of NPK (S) (15-15-15 (10)) at a dose of 200kg/ha. The profitability level of this fertilizer was 88,9%.


1998 ◽  
Vol 37 (4II) ◽  
pp. 873-882 ◽  
Author(s):  
Sarfaraz Khan Quershi

Growth in telecom infrastructure and provision of modern telecom services to consumers at a cost based tariff helps growth of national economy. Modern telecoms serve as the engine of growth of national economy. Following the global trends of liberalisation and deregulation in telecoms monopolies which have thus far been providing inefficient communication at a greedily high tariffs are falling apart. Mergers in telecoms are not for increasing the size of the monopoly but to provide more efficient and cost effective services to the consumers. In Pakistan the erstwhile T&T department played a needful role at its time. Conversion of the department into a corporation and then into a company were steps necessary for following the global trends. Need now is to continue this trend further, eliminate the monopolistic approach by allowing more players in the field thus permitting the market forces to decide the provision of better quality of modern services at competitive price.


Author(s):  
Gwee Hoon Yen ◽  
Ng Kiong Kay

Abstract Today, failure analysis involving flip chip [1] with copper pillar bump packaging technologies would be the major challenges faced by analysts. Most often, handling on the chips after destructive chemical decapsulation is extremely critical as there are several failure analysis steps to be continued such as chip level fault localization, chip micro probing for fault isolation, parallel lapping [2, 3, 4] and passive voltage contrast. Therefore, quality of sample preparation is critical. This paper discussed and demonstrated a quick, reliable and cost effective methodology to decapsulate the thin small leadless (TSLP) flip chip package with copper pillar (CuP) bump interconnect technology.


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