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Integrating Immunotherapy and Nanotechnology in Advanced Drug Delivery Systems for Precision Cancer Therapy 将免疫疗法和纳米技术整合到先进的给药系统中,实现癌症精准治疗
Pub Date : 2024-01-13 DOI: 10.61427/jcpr.v4.i1.2024.119
V. Jyothi Krishna, L. Swathi, S. S. Lakshmi
This review article investigates recent advancements in drug delivery systems, with a specific emphasis on integrating nanotechnology and immunotherapy for precision cancer therapy. This review explores the design, development, and optimization of novel drug delivery platforms aimed at improving drug efficacy, minimizing side effects and enhancing patient outcomes. The synergistic interplay between nanocarriers and immunotherapeutic agents shows significant potential in addressing current challenges in cancer treatment, such as drug resistance and off-target effects. This article reviews recent preclinical and clinical studies, highlighting the transformative potential of these innovative approaches to reshape cancer therapeutics and facilitate the advent of personalized medicine in oncology. The research findings contribute to the ongoing initiatives aimed at refining the effectiveness and safety of pharmaceutical interventions, bringing us one step closer to more efficient and targeted cancer treatments.
这篇综述文章探讨了给药系统的最新进展,特别强调了纳米技术与免疫疗法在癌症精准治疗中的结合。这篇综述探讨了新型给药平台的设计、开发和优化,旨在提高药物疗效、减少副作用和改善患者预后。纳米载体与免疫治疗药物之间的协同作用在应对当前癌症治疗的挑战(如耐药性和脱靶效应)方面显示出巨大的潜力。本文回顾了最近的临床前和临床研究,强调了这些创新方法在重塑癌症疗法和促进肿瘤学中个性化医疗的出现方面所具有的变革潜力。这些研究成果有助于不断完善药物干预的有效性和安全性,使我们离更高效、更有针对性的癌症治疗更近一步。
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引用次数: 0
Impact of Gene Therapy and Genetic Mutations in Rare Diseases 基因治疗和基因突变对罕见病的影响
Pub Date : 2024-01-13 DOI: 10.61427/jcpr.v4.i1.2024.118
V. Jyothi Krishna, Ch. Kesari
This article provides a thorough examination of recent progress in gene therapy as a transformative avenue for treating rare diseases characterized by genetic mutations. The authors explore fundamental principles of gene therapy, encompassing both viral and non-viral vectors employed for efficient gene delivery. This article delves into the potential of state-of-the-art genome-editing technologies, such as CRISPR/Cas9, to rectify genetic abnormalities, emphasizing their precision and scalability. Regulatory considerations and ethical implications surrounding gene therapy are discussed, underlining the importance of a balanced and responsible approach in translating these innovations into clinical practice. As gene therapy continues to evolve, its expanding role in addressing rare diseases offers hope to individuals grappling with these complex conditions.
基因疗法是治疗以基因突变为特征的罕见病的一种变革性途径,本文对基因疗法的最新进展进行了深入探讨。作者探讨了基因治疗的基本原理,包括用于有效传递基因的病毒载体和非病毒载体。本文深入探讨了 CRISPR/Cas9 等最先进的基因组编辑技术在纠正基因异常方面的潜力,强调了这些技术的精确性和可扩展性。文章讨论了基因疗法的监管因素和伦理影响,强调了在将这些创新技术转化为临床实践时采取平衡、负责任的方法的重要性。随着基因疗法的不断发展,它在治疗罕见病方面的作用也在不断扩大,这为与这些复杂疾病作斗争的人们带来了希望。
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引用次数: 0
Plummer-Vinson Syndrome: A Rare Case Report 普卢默-文森综合征:罕见病例报告
Pub Date : 2024-01-13 DOI: 10.61427/jcpr.v4.i1.2024.115
Mukesh Kumar Saphi, Yalla Sai Vijaya Durga, Sunny Kumar Yadav, Krishnadev Shah, Amit Kumar
Plummer-Vinson syndrome, also called Paterson-Kelly syndrome, is characterized by the classic triad of dysphagia, iron-deficiency anemia, and esophageal webs. This syndrome is associated with an increased incidence of post-cricoid carcinoma and for surveillance, an endoscopy is recommended under general anesthesia. This was a case of 74-year-old woman with Plummer-Vinson Syndrome who was successfully treated with Savary-Gilliard (SG) dilation or Esophageal dilation. The patient had a long-standing clinical history of iron deficiency anemia with slow progression of dysphagia of solid food from 10 years and glossoepiglotic fold, aryepiglottic fold bilaterally arytenoid on the left & right side and had experienced difficulty in swallowing for the past 10 years. Along with this patient is having abdominal pain radiating to the epigastrium region and fever with chills & rigors. An endoscopy examination was conducted under general anesthesia and revealed the esophageal web at the level of the cervical esophagus. Laboratory data investigation shows an RBC count of 2.09 million/cumm, haemoglobin of 6.6 gm/dl%, and serum iron of 7µg/dl. The patient was prescribed Inj. Orofer-XT 100 mg intravenous iron sucrose supplement daily for 15 days, Inj. Pantoprazole 40 mg daily for 1 week, Inj. Tramadol 1amp whenever required and Syp.Sucralfate 15 ml 30 minutes before food. Her anemia condition was improved but dysphagia did not improve. To treat dysphagia the Savary-Gilliard (SG) dilation was done under fluoroscopy by endoscopically a single session was performed that serially increased the diameter by disrupting the web without any complication. After SG-dilation, the patient's dysphagia resolved shortly after the treatment.
普卢默-文森综合征又称帕特森-凯利综合征,其特征是典型的吞咽困难、缺铁性贫血和食管蹼三联征。该综合征与环状带后癌的发病率增加有关,为进行监测,建议在全身麻醉下进行内窥镜检查。这是一例患有普卢默-文森综合征的 74 岁女性患者,她成功地接受了萨瓦里-吉利尔德(SG)扩张术或食管扩张术。患者有长期缺铁性贫血的临床病史,从 10 年前开始出现吞咽固体食物困难的缓慢进展,左侧和右侧有舌咽神经褶、双侧杓状舌骨褶,过去 10 年来一直有吞咽困难。此外,患者还伴有腹痛,并向上腹放射,发热、畏寒和全身僵硬。内窥镜检查是在全身麻醉的情况下进行的,结果显示颈部食管处有食管网。实验室数据调查显示,红细胞计数为 209 万/立方厘米,血红蛋白为 6.6 克/分升,血清铁为 7 微克/分升。医生给患者开了 Inj.Orofer-XT 100 毫克,每天静脉注射蔗糖铁补充剂,持续 15 天;Inj.泮托拉唑 40 毫克,每天一次,持续 1 周。曲马多注射液 1 安培,饭前 30 分钟服用。她的贫血状况有所改善,但吞咽困难没有改善。为了治疗吞咽困难,在透视下通过内窥镜进行了萨瓦里-吉利尔德(SG)扩张术,该手术只进行了一次,通过破坏网状结构连续增加了直径,没有出现任何并发症。SG扩张术后,患者的吞咽困难很快就得到了缓解。
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引用次数: 0
A Review on Innovative Drug Delivery Platforms 创新给药平台综述
Pub Date : 2024-01-13 DOI: 10.61427/jcpr.v4.i1.2024.120
Slesha Kumar Kosuru, V. S. Rao, K.V.S.S. Annapurna, Bhagya Naga, Lakshmi Siripalli, D.Sri, Sai Sukruta, B. Tharuna, Mr. Slesha, Kumar Kosuru, M.Pharm
In recent years, the field of drug delivery has undergone a transformative shift with the introduction of innovative platforms that transcend conventional methods, providing accurate and efficient means for delivering therapeutic agents. This exploration delves into the distinctive features and potential impacts of these pioneering platforms, charting a course for the future of pharmaceutical interventions. In this review article, the advancements regarding the nanotechnology-enabled delivery, lipid-based drug delivery systems, targeted drug delivery, implantable drug delivery systems, 3D printing in drug delivery, stimuli-responsive delivery systems, mRNA and gene delivery platforms and microfluidic - based delivery systems were discussed. These innovative drug delivery platforms represent a dynamic frontier in pharmaceutical research and development. They afford unprecedented control over drug properties, release kinetics and targeting strategies. As research continues to push the boundaries of drug delivery science, these innovations hold the potential to revolutionize the treatment of various diseases, ushering in safer, more effective and patient-centric therapeutic solutions.
近年来,随着超越传统方法的创新平台的推出,药物输送领域经历了一场变革,为治疗药物的输送提供了准确而高效的手段。本文将深入探讨这些先锋平台的独特之处和潜在影响,为未来的药物干预指明方向。在这篇综述文章中,讨论了纳米技术驱动的给药、脂质给药系统、靶向给药、植入式给药系统、3D 打印给药系统、刺激响应式给药系统、mRNA 和基因给药平台以及基于微流体的给药系统等方面的进展。这些创新的给药平台代表了制药研发领域的一个动态前沿。它们可以对药物特性、释放动力学和靶向策略进行前所未有的控制。随着研究工作不断推动给药科学的发展,这些创新技术有可能彻底改变各种疾病的治疗方法,带来更安全、更有效和以病人为中心的治疗方案。
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引用次数: 0
Precision Pharmacogenomics: A Review 精准药物基因组学:综述
Pub Date : 2024-01-13 DOI: 10.61427/jcpr.v4.i1.2024.121
Slesha Kumar Kosuru, Santhosh Gandham, Bhagya Naga Lakshmi Siripalli, K.V.S.S. Annapurna, D. Vinoothna, D. Vaishnavi
Embarking on precision pharmacogenomics journey is a transformative experience in the world of medicine. This innovative approach, distinct from traditional practices tailors treatments to each individual's unique genes. Unlike standard methods where everyone gets the same medicine, precision pharmacogenomics uses a person's genetic information as an approach to determine the most effective treatment. In this personalized medical adventure, the individual's genes act like a guide for healthcare providers. Moreover, there is a growing focus on ensuring equitable access to personalized medicine. Efforts to address healthcare disparities and promote inclusivity in genomic research are expected to take center stage. Ethical considerations and robust regulatory frameworks will play pivotal roles in guiding the responsible and transparent application of precision pharmacogenomics. The future of precision pharmacogenomics promises a healthcare landscape where treatments are finely tuned to the unique genetic makeup of each individual. This forward-looking perspective suggests a future characterized by enhanced effectiveness, reduced side effects and a more inclusive approach to personalized healthcare.
踏上精准药物基因组学之旅,是医学界的一次变革。这种有别于传统做法的创新方法根据每个人的独特基因量身定制治疗方案。与每个人都服用同一种药物的标准方法不同,精准药物基因组学利用个人的基因信息来确定最有效的治疗方法。在这种个性化医疗探险中,个人基因就像医疗服务提供者的指南。此外,确保公平获得个性化医疗服务也日益受到关注。在基因组研究中,解决医疗差距和促进包容性的努力预计将占据中心位置。伦理因素和健全的监管框架将在指导负责任和透明地应用精准药物基因组学方面发挥关键作用。精准药物基因组学的未来将是一个根据每个人独特的基因构成对治疗方法进行微调的医疗环境。这一前瞻性视角预示着未来将以提高疗效、减少副作用和采用更具包容性的个性化医疗方法为特征。
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引用次数: 0
A Brief Review on Analytical Techniques in Bioequivalence Studies 生物等效性研究中的分析技术简评
Pub Date : 2024-01-13 DOI: 10.61427/jcpr.v4.i1.2024.117
Slesha Kumar Kosuru, Tadi Suvarna Kosuru, Gunapati Jyothi, Kandregula Sai Siva Saran, Polinati Syam Sundhar
In the pharmaceutical research and development, bioequivalence studies hold a critical position, serving as a vital component in evaluating the equivalence of generic drugs with their reference counterparts. These studies, which examine the interchangeability between generic and brand-name medications, depend heavily on a range of analytical techniques to measure the presence and concentration of a drug's active pharmaceutical ingredient (API) within the human body. The comprehensive use of these analytical methods ensures the confidence of healthcare providers and regulatory bodies in the effectiveness, quality and safety of generic medications. The field of pharmaceutical analysis is dynamic and forward-looking, with analysts, researchers and scientists energetically engaged in forging a future characterized by ground breaking discoveries and refined pharmaceutical solutions. This is a realm where scientific excellence and innovation harmonize, ultimately benefiting the health and welfare of individuals and societies across the globe. The key takeaways underscore the field's resilience and its unwavering commitment to upholding the highest standards in drug development and quality control while pioneering cutting-edge technologies with the promise of safer, more effective pharmaceuticals for all.
在医药研发领域,生物等效性研究占据着重要地位,是评估仿制药与其参照药等效性的重要组成部分。这些研究主要考察仿制药和品牌药之间的互换性,主要依靠一系列分析技术来测量药物活性药物成分 (API) 在人体内的存在和浓度。这些分析方法的全面使用确保了医疗服务提供者和监管机构对仿制药有效性、质量和安全性的信心。药物分析领域是一个充满活力和前瞻性的领域,分析师、研究人员和科学家们都在以突破性的发现和完善的药物解决方案为特点,积极地参与到未来的建设中。这是一个科学卓越与创新和谐共存的领域,最终将惠及全球个人和社会的健康与福祉。会议的主要收获强调了这一领域的韧性和坚定不移的承诺,即坚持药物开发和质量控制的最高标准,同时开拓前沿技术,为所有人提供更安全、更有效的药物。
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引用次数: 0
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Journal of Clinical and Pharmaceutical Research
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