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標(biāo)題: Titlebook: Drug Delivery Systems; Kewal K. Jain Book 2020Latest edition Springer Science+Business Media, LLC, part of Springer Nature 2020 Targeted d [打印本頁(yè)]

作者: VER    時(shí)間: 2025-3-21 18:04
書(shū)目名稱Drug Delivery Systems影響因子(影響力)




書(shū)目名稱Drug Delivery Systems影響因子(影響力)學(xué)科排名




書(shū)目名稱Drug Delivery Systems網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱Drug Delivery Systems網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱Drug Delivery Systems被引頻次




書(shū)目名稱Drug Delivery Systems被引頻次學(xué)科排名




書(shū)目名稱Drug Delivery Systems年度引用




書(shū)目名稱Drug Delivery Systems年度引用學(xué)科排名




書(shū)目名稱Drug Delivery Systems讀者反饋




書(shū)目名稱Drug Delivery Systems讀者反饋學(xué)科排名





作者: 朦朧    時(shí)間: 2025-3-21 22:42
978-1-4939-9800-5Springer Science+Business Media, LLC, part of Springer Nature 2020
作者: 慌張    時(shí)間: 2025-3-22 01:28
,Synthesis of Gold Nanoparticle: Peptide–Drug Conjugates for Targeted Drug Delivery,e their stability in biological solutions. Here we describe an effective method to easily couple PDCs to polyethylene-coated gold nanoparticles. We also outline analytical methods to validate the coupling and assays to measure the stability and cytotoxic efficacy of the conjugates.
作者: 寬度    時(shí)間: 2025-3-22 04:44
Vorposten der Gesundheitspflegen described as well as devices used for drug delivery and targeted drug delivery. There has been a considerable increase in the number of new biotechnology-based therapeutics. Most of these are proteins and peptides, and their delivery present special challenges. Cell and gene therapies are sophisti
作者: Hla461    時(shí)間: 2025-3-22 11:31

作者: 清楚說(shuō)話    時(shí)間: 2025-3-22 16:38
Handbibliothek für Bauingenieure are pierced to enter the intrathecal space. The dural sac is mostly constituted by the outer layer of dura and the inner layer called arachnoid membrane, which regulates diffusion of drugs into the intrathecal space. The pia matter surrounding the spinal cord is a permeable structure allowing the p
作者: 清楚說(shuō)話    時(shí)間: 2025-3-22 20:21
https://doi.org/10.1007/978-3-662-40050-0he central nervous system (CNS), in particular, has remained a challenge for drug delivery. This is mainly due to barriers such as the blood–brain barrier (BBB) and blood–cerebrospinal fluid barrier (BCSFB), which hinder drug molecules from reaching the brain and spinal cord tissue. Although researc
作者: 消耗    時(shí)間: 2025-3-22 22:56
George L. Maddox,M. Powell Lawtone their stability in biological solutions. Here we describe an effective method to easily couple PDCs to polyethylene-coated gold nanoparticles. We also outline analytical methods to validate the coupling and assays to measure the stability and cytotoxic efficacy of the conjugates.
作者: chapel    時(shí)間: 2025-3-23 02:24

作者: Analogy    時(shí)間: 2025-3-23 09:00

作者: 引導(dǎo)    時(shí)間: 2025-3-23 11:34
Affine und projektive Geometrieuse of cancer-related death in both men and women. Nonetheless, there has been no significant improvement in survival for pancreatic ductal adenocarcinoma (PDAC) patients over the past 30+ years. For this reason, there is a considerable and urgent clinical need to develop innovative strategies for e
作者: 變形    時(shí)間: 2025-3-23 16:10

作者: harbinger    時(shí)間: 2025-3-23 20:47
Des Kurpfuschers Abschied an seinen Sohn to the pharmaceutical formulation of taxanes are still a reality and mainly due to the low aqueous solubility of these medicines, as well as to the nontargeted therapy and consequent side effects. Nanoparticles (NPs) of poly(lactic-co-glycolic acid) (PLGA) and polyethylene glycol (PEG) have sparked
作者: Cacophonous    時(shí)間: 2025-3-23 22:44
Des Kurpfuschers Abschied an seinen Sohnllenging due to barrier provided by the top layer of skin known as stratum corneum (SC). The chemical permeation enhancers or specialized carriers such as nanoparticles (NPs) are needed which can deliver drug molecules into the deeper layer..Here, we describe the in silico design of nanoparticle car
作者: 遺忘    時(shí)間: 2025-3-24 03:22

作者: myelography    時(shí)間: 2025-3-24 09:23
Des Kurpfuschers Abschied an seinen Sohne for a widespread use of siRNAs in the clinics. Solid lipid-based nanoparticles (SLNs) and derivatives can potentially fit this purpose by enabling to overcome the extracellular and intracellular physiological barriers affecting the delivery. For that, rational formulations and rational process des
作者: 取之不竭    時(shí)間: 2025-3-24 11:27

作者: 本土    時(shí)間: 2025-3-24 17:30

作者: 凹槽    時(shí)間: 2025-3-24 22:42
Drug Delivery Systems978-1-4939-9798-5Series ISSN 1064-3745 Series E-ISSN 1940-6029
作者: gruelling    時(shí)間: 2025-3-25 02:31

作者: 冷漠    時(shí)間: 2025-3-25 06:17

作者: MOT    時(shí)間: 2025-3-25 08:07
Methods in Molecular Biologyhttp://image.papertrans.cn/e/image/283040.jpg
作者: 牽索    時(shí)間: 2025-3-25 12:32

作者: jagged    時(shí)間: 2025-3-25 19:51

作者: VEIL    時(shí)間: 2025-3-25 23:43
Des Kurpfuschers Abschied an seinen Sohnigns are needed. This chapter addresses a comprehensive description and critical appraisal of the main production methods of this particular type of lipid nanoparticles and the leading strategies to prompt a targeted delivery of siRNA.
作者: Diverticulitis    時(shí)間: 2025-3-26 01:56
Book 2020Latest editionpics such as drug delivery in cancer and intrathecal delivery of analgesics in humans. The increasing role of nanobiotechnology is reflected in eight of the sixteen chapters that include synthesis of gold nanoparticles; targeted siRNA delivery; and lipid nanocarriers. Written in the highly successfu
作者: debunk    時(shí)間: 2025-3-26 04:24

作者: neutrophils    時(shí)間: 2025-3-26 11:16
Vorposten der GesundheitspflegeDrug delivery to the brain across the blood–brain barrier presents many challenges. Refinements in drug delivery will facilitate the development of personalized medicine. The ideal DDS is defined. Commercial aspects, challenges, and future of DDSs are discussed.
作者: 含沙射影    時(shí)間: 2025-3-26 16:02
https://doi.org/10.1007/978-3-662-40050-0ons, and for enhancement of medical imaging. We look at the problems and recent advances in the development of nanoparticles for spine-related applications and provide a comprehensive review on recent research work.
作者: 天文臺(tái)    時(shí)間: 2025-3-26 18:36
Des Kurpfuschers Abschied an seinen Sohnoneedles are very short and sharp needles which do not cause pain. Thus, in the present investigation, preparation and evaluation of a transdermal delivery system for tizanidine hydrochloride based on microneedles are described.
作者: Little    時(shí)間: 2025-3-26 21:40
Vorposten der Gesundheitspflegeation and characterization of nanostructured lipid carriers of temozolomide, a chemotherapeutic drug. Evaluation of pharmacokinetics and biodistribution of the nanocarrier system in rats revealed improved delivery of the chemotherapeutic agent to the brain with the potential of lesser side effects.
作者: 蜈蚣    時(shí)間: 2025-3-27 01:42

作者: 爵士樂(lè)    時(shí)間: 2025-3-27 07:00
An Overview of Drug Delivery Systems,Drug delivery to the brain across the blood–brain barrier presents many challenges. Refinements in drug delivery will facilitate the development of personalized medicine. The ideal DDS is defined. Commercial aspects, challenges, and future of DDSs are discussed.
作者: SAGE    時(shí)間: 2025-3-27 13:32

作者: 類似思想    時(shí)間: 2025-3-27 13:38
Microneedle-Mediated Transdermal Delivery of Tizanidine Hydrochloride,oneedles are very short and sharp needles which do not cause pain. Thus, in the present investigation, preparation and evaluation of a transdermal delivery system for tizanidine hydrochloride based on microneedles are described.
作者: 可忽略    時(shí)間: 2025-3-27 19:25
Lipid Nanocarriers for Enhanced Delivery of Temozolomide to the Brain,ation and characterization of nanostructured lipid carriers of temozolomide, a chemotherapeutic drug. Evaluation of pharmacokinetics and biodistribution of the nanocarrier system in rats revealed improved delivery of the chemotherapeutic agent to the brain with the potential of lesser side effects.
作者: 無(wú)可非議    時(shí)間: 2025-3-28 01:13
Construction of a Macrophage-Targeting Bio-nanocapsule-Based Nanocarrier,followed by size exclusion column chromatography. In addition, GL-BNCs can be fused with liposomes to form GL-virosome. The targeted delivery of GL-BNC and GL-virosome to macrophages can be confirmed by in vitro phagocytosis assays using the murine macrophage cell line RAW264.7.
作者: Pcos971    時(shí)間: 2025-3-28 05:34
1064-3745 ation advice from the expertsThis third edition volume expands on the previous editions with a discussion of new and updated methods used to study drug delivery. Chapters cover topics such as drug delivery in cancer and intrathecal delivery of analgesics in humans. The increasing role of nanobiotech
作者: 磨坊    時(shí)間: 2025-3-28 06:19
Preparation of Cholera Toxin Subunit B Functionalized Nanoparticles for Targeted Therapy of Glioblaque modification can guide nanoparticles across the BBB and target glioblastoma cells. The characterization of nanoparticles such as size, zeta potential, morphology, drug loading, and encapsulation efficiency is shown in this chapter.
作者: 一大塊    時(shí)間: 2025-3-28 11:22

作者: 高調(diào)    時(shí)間: 2025-3-28 18:01
Targeted siRNA Delivery Using Lipid Nanoparticles,igns are needed. This chapter addresses a comprehensive description and critical appraisal of the main production methods of this particular type of lipid nanoparticles and the leading strategies to prompt a targeted delivery of siRNA.
作者: Opponent    時(shí)間: 2025-3-28 20:31
https://doi.org/10.1007/978-3-662-39988-0 new recommendations that may improve outcomes. This chapter reviews all technological issues regarding IDDS implantation with follow-up and pharmacological recommendations published during recent years that provide evidence-based decision-making process in the management of chronic pain and spasticity in patients.
作者: Accolade    時(shí)間: 2025-3-28 23:01
Handbibliothek für Bauingenieurethecal catheter which can cause damage to nerve roots and spinal cord. Multiple factors may be involved in the mechanisms of drug diffusion across the membranes of the spinal cord, as well as in their dilution with the CSF, which will lead to the final drug distribution and availability at nerve roots and the spinal cord.
作者: 流動(dòng)才波動(dòng)    時(shí)間: 2025-3-29 06:58
Fredric D. Wolinsky Ph.D.,Connie Lea Arnoldd from degradation but also to selectively deliver the siRNA to transferrin receptor (TfR)-overexpressing cells, playing key roles in the pathology of numerous cancer types as well as inflammatory diseases.
作者: declamation    時(shí)間: 2025-3-29 09:49
Intrathecal Drug Delivery, new recommendations that may improve outcomes. This chapter reviews all technological issues regarding IDDS implantation with follow-up and pharmacological recommendations published during recent years that provide evidence-based decision-making process in the management of chronic pain and spasticity in patients.
作者: INCH    時(shí)間: 2025-3-29 12:15
Microanatomy Relevant to Intrathecal Drug Delivery,thecal catheter which can cause damage to nerve roots and spinal cord. Multiple factors may be involved in the mechanisms of drug diffusion across the membranes of the spinal cord, as well as in their dilution with the CSF, which will lead to the final drug distribution and availability at nerve roots and the spinal cord.
作者: machination    時(shí)間: 2025-3-29 18:53
A Method for Targeted Nonviral siRNA Delivery in Cancer and Inflammatory Diseases,d from degradation but also to selectively deliver the siRNA to transferrin receptor (TfR)-overexpressing cells, playing key roles in the pathology of numerous cancer types as well as inflammatory diseases.
作者: Mediocre    時(shí)間: 2025-3-29 23:21

作者: 流利圓滑    時(shí)間: 2025-3-30 00:41

作者: Observe    時(shí)間: 2025-3-30 05:33

作者: 哪有黃油    時(shí)間: 2025-3-30 12:13
Drug Delivery Applications of Nanoparticles in the Spine,he central nervous system (CNS), in particular, has remained a challenge for drug delivery. This is mainly due to barriers such as the blood–brain barrier (BBB) and blood–cerebrospinal fluid barrier (BCSFB), which hinder drug molecules from reaching the brain and spinal cord tissue. Although researc
作者: 盡責(zé)    時(shí)間: 2025-3-30 16:27
,Synthesis of Gold Nanoparticle: Peptide–Drug Conjugates for Targeted Drug Delivery,e their stability in biological solutions. Here we describe an effective method to easily couple PDCs to polyethylene-coated gold nanoparticles. We also outline analytical methods to validate the coupling and assays to measure the stability and cytotoxic efficacy of the conjugates.
作者: MEET    時(shí)間: 2025-3-30 19:57
A Method for Targeted Nonviral siRNA Delivery in Cancer and Inflammatory Diseases,otentially silence any chosen gene. Nevertheless, efficient delivery still presents a major hurdle to translating this promising technology into medical practice. Here, we describe a straightforward method to prepare and characterize an effective delivery system consisting of low-molecular-weight po
作者: BAN    時(shí)間: 2025-3-31 00:07





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