Pharmaceutical Nanotechnology - Online First
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Current Updates on Nanotechnology-based Drug Delivery Platforms for Treating Alzheimer’s with Herbal Drugs
Available online: 23 December 2024More LessAlzheimer's disease (AD) is an irreversible brain disorder that led to memory loss and disrupts daily life. Earlier strategies to treat AD such as acetylcholinesterase inhibitor (AChEI) drugs are not showing effectiveness due to the inability to cross the blood-brain barrier. Moreover, traditional AChEI provides limited efficacy in terms of bioavailability and solubility for treating AD treatment. Many of the current drugs such as donepezil taken to treat the disease exhibited harmful side effects. Hence, researchers are keen to find the alternative effective therapeutic agents for treating AD. This review summarizes the recent advancement in nanotechnology-based drug delivery systems of herbal drugs such as Curcumin, Ginkgo biloba, Salvia officinalis, etc for the prevention and cure of AD. Herbal drugs proved useful in treating neuronal disorders such as AD but exhibited some limitations like low bioavailability via oral drug delivery. Such limitations were overcome by tagging these drugs by nanoparticles which enables them to cross the blood-brain barrier and offer the delivery of greater concentration of herbal drugs to the brain. Inorganic nanoparticle-based drug-delivery systems such as gold nanoparticles and magnetic nanoparticles, organic nanoparticulate systems like polymeric micelles and dendrimers, and solid polymeric nanoparticles were some of the effective methods that have earlier shown potential for enhancing the delivery of herbal drugs to the brain. Long-term repeated injection of drugs loaded on nanomaterials can lead to the accumulation of nanomaterials in the body without timely and effective degradation which can cause serious issues to the brain. Hence, nanotechnology-based strategies should involve the formulation of non-toxic nanoparticles in such a way that they can significantly transport the drugs across the BBB followed by effective degradation of nanoparticles.
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Formulation, Development, and Optimization of Fast Dissolving Tablets Containing Tapentadol Hydrochloride
Available online: 23 December 2024More LessBackgroundTapentadol hydrochloride is a potent analgesic commonly used to manage moderate to severe pain. Rapidly dissolving tablets of Tapentadol offer a significant advantage in enhancing patient compliance by providing quick pain relief. The development of fast-dissolving tablets (FDTs) requires careful consideration of formulation parameters to achieve optimal disintegration and dissolution profiles. In this study, the aim was to fabricate Tapentadol FDTs by selecting suitable super disintegrating agents such as croscarmellose sodium and crospovidone, which serve as two independent variables. The direct compression method was employed to formulate nine different Tapentadol hydrochloride formulations (TH1 to TH9).
Materials and MethodsThe study utilized Design-Expert® software version 13.0 and the Response Surface Methodology (RSM) for the optimization of Tapentadol FDTs. The formulations were prepared using the direct compression method with varying concentrations of the super disintegrants, croscarmellose sodium, and crospovidone. The primary response variables considered in this optimization study included disintegration time (Y1), percentage drug release at 15 minutes (Q15, Y2), and percentage drug release at 30 minutes (Q30, Y3). All pre-compressional and post-compressional parameters were evaluated for each formulation, along with in vitro dissolution studies. Furthermore, DD Solver, a statistical tool, was employed to determine the kinetics of drug release and the release order mechanism based on regression coefficient value (r2), Akaike Information Criterion (AIC), and Model Selection Criteria (MSC).
ResultsThe evaluation studies indicated that the TH5 formulation exhibited the most rapid disintegration time and the highest drug release percentage within the specified time frame. The super disintegrants used demonstrated a significant impact on the response variables, notably enhancing the solubility and dissolution rate of Tapentadol hydrochloride. Based on the exponent release (n) value, the study concluded that the TH5 formulation followed a first-order release kinetics and Fickian diffusion mechanism for drug release. Stability studies were performed following the International Council for Harmonization (ICH) guidelines to assess the shelf-life of the optimized formulation. The ANOVA data revealed that the p-value was greater than 0.05, indicating no significant differences during the storage period. Additionally, a similarity factor (f2) analysis was conducted to compare the optimized formulation with the marketed formulation (Tydol 100 mg).
DiscussionThe findings highlight the crucial role of super disintegrants in fast-dissolving tablet formulation, significantly impacting disintegration time and dissolution profile. The TH5 formulation excelled in rapid disintegration and drug release, optimized using RSM and Design-Expert software, with statistical analysis confirming the Fickian diffusion mechanism for drug release.
ConclusionThe study successfully developed and optimized Tapentadol fast-dissolving tablets using direct compression and response surface methodology. The TH5 formulation showed rapid disintegration and optimal drug release, with stability confirmed under ICH conditions. This highlights the importance of super disintegrants in FDT formulation for rapid action and patient compliance.
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A Critical Review on Lipid Nanoparticle-based siRNA Formulations for Breast Cancer Management
Authors: Phool Chandra, Vaibhav Rastogi, Mayur Porwal, Himanshu Sharma, Anurag Verma and Neetu SachanAvailable online: 12 December 2024More LessBreast cancer poses a formidable challenge due to its inherent difficulty in treatment. Recognizing the imperative need for new therapeutic approaches, this study focuses on a groundbreaking technique that has the potential to reshape breast cancer treatment: siRNA formulations based on lipid nanoparticles (LNPs). This novel method holds promise for transforming the landscape of breast cancer therapy. The primary objective of this research is to conduct a comprehensive assessment of the current state of the art in the field, specifically exploring the potential applications of siRNA treatments encapsulated in LNPs for breast cancer. The research methodology involves a detailed literature review covering breast cancer, siRNA therapy, and lipid nanoparticles. The study investigates the fundamental principles of siRNA therapy, highlighting its capacity to selectively silence genes critical to breast cancer development. Additionally, the application of LNPs in delivering therapeutic siRNA payloads is explored, with an emphasis on the benefits of LNPs, including their biocompatibility and effective siRNA incorporation. Safety and effectiveness characteristics of LNP-based siRNA formulations are also assessed to pave the way for potential therapeutic applications. Findings from the study illuminate the promising characteristics of LNP-siRNA formulations in the treatment of breast cancer. The investigation provides insights into targeting strategies, such as the enhanced permeability and retention (EPR) effect and the utilization of ligand-conjugated nanoparticles. The study outlines potential avenues for therapeutic use, drawing attention to the safety and effectiveness of LNP-based siRNA formulations. In summary, this study aims to reveal intricate interactions between lipid nanoparticle-based siRNA formulations and breast cancer treatment, fostering a transformation in the field by highlighting current developments, future trends, and innovative strategies for next-gen LNP-based siRNA formulations.
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Biological Synthesis of Metallic Nanoparticles: Latest Insights and Applications
Authors: Khadija El Ouardy, Hassan Ahmoum and Youssef MirAvailable online: 12 December 2024More LessNanotechnology is rapidly transforming various fields, including medicine, environmental conservation, agriculture, and pharmaceuticals. The production of metallic nanoparticles is a key area within this field, known for its innovative applications. However, traditional chemical and physical methods used for nanoparticle synthesis often involve toxic chemicals and are expensive, making them unsuitable for large-scale production. To address these issues, there has been a growing focus on developing sustainable, cost-effective, and eco-friendly methods. One promising approach is the biological synthesis of metallic nanoparticles. This technique combines principles from biology and nanotechnology, using natural sources such as plant extracts, bacteria, fungi, yeast, and algae to produce nanoparticles in an environmentally friendly way. This review examines the biological synthesis of various metal nanoparticles, including platinum, palladium, gold, and silver. It explores different green methods used for their production and discusses the mechanisms that enable these biological processes. Additionally, the review highlights the diverse applications of these nanoparticles, from environmental cleanup and heavy metal removal to cancer treatment and drug delivery. By focusing on green synthesis methods, this approach not only reduces environmental impact but also offers a scalable, sustainable alternative to traditional nanoparticle production techniques. As research in this area advances, these eco-friendly methods are expected to play a crucial role in the future of nanotechnology.
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Solid Lipid Nanoparticles and Nanostructured Lipid Particles: A Comparative Review on Lipid-Based Nanocarriers
Authors: Anjali Sharma, Devkant Sharma, Pritish Kumar Panda and Niladry GhoshAvailable online: 10 December 2024More LessLipid-based nanocarriers have emerged as promising vehicles for the delivery of various therapeutic agents, owing to their biocompatibility, stability, and ability to encapsulate both hydrophilic and hydrophobic drugs. Among these lipid-based nanocarriers, Solid Lipid Nanoparticles (SLNs) and Nanostructured Lipid Carriers (NLCs) have gained significant attention in the field of drug delivery. This comparative review aims to provide a comprehensive analysis of SLNs and NLCs, focusing on their formulation, physicochemical properties, drug-loading capacity, stability, and drug release profiles. The review highlights the differences in preparation techniques, particle size, zeta potential, drug encapsulation efficiency, stability, drug delivery, cosmetic and personal care, and food industry applications between SLN and NLC. Furthermore, the review discusses the toxicity and safety profiles of these nanoparticles, including cytotoxicity, genotoxicity, acute toxicity, and long-term toxicity. Finally, the review identifies the potential applications, limitations, and future research directions of SLN and NLC.In summary, this comparative review provides valuable insights into the formulation, physicochemical properties, drug-loading capacity, stability, and drug release profiles of SLNs and NLCs. By understanding the similarities and differences between these lipid-based nanocarriers, researchers and pharmaceutical scientists can make informed decisions regarding the selection of the most suitable nanocarrier for specific therapeutic applications.
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Network Pharmacology and Optimization of β-Sitosterol-Loaded Solid Lipid Nanoparticles Using Box-Behnken Design for Enhanced Solubility and Sustained Drug Release in Diabetes
Authors: Ramsha Aslam, Varsha Tiwari, Prashant Upadhyay and Abhishek TiwariAvailable online: 10 December 2024More LessIntroductionThe pharmaceutical industry has paid a lot of attention to solid lipid nanoparticles (SLN) because they show promising drug delivery vehicles.
MethodThis work aimed to design and optimize the SLN of β-sitosterol, a hydrophobic drug, to improve solubility and sustained action. An ultrasonication technique after melting was used to design SLN using a randomized response surface Box-Behnken design (BBD). Network pharmacology analysis was performed to explore the interactions between genes. According to the findings, Compritol ATO 888 was the most soluble at a drug: lipid ratio of 1:3. Particle size, PDI, zeta, and entrapment efficiency (EE) were observed as 168.83nm, 0.231 -28.9 Mv, and 68.29%, respectively. The optimized formulation did not undergo any chemical changes, as depicted through DSC. The in vitro drug release investigation showed that the SLN released the drug continuously for 28 hours. Scanning Electron Microscopy (SEM) revealed homogenous, spherical particles.
ResultThe antidiabetic potential of the formulation was assessed through the potential of glucose uptake by yeast, and the α-amylase inhibitory assay revealed its significant antidiabetic potential when compared with that of the standard drug metformin. The network pharmacology of β-sitosterol demonstrated gene interaction with hexokinase, phosphoglucomutases, glucose-6-phosphate dehydrogenase, hexose-6-phosphate dehydrogenase, and glutathione disulfide reductase.
ConclusionThe β-sitosterol-loaded SLN generated by BBD was found to be a potential method for improving drug solubility with sustained drug release and was found to be long-term storage stable.
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Green Synthesis of Curcumin-Loaded Bacterial Nanocellulose for Topical Application: Preparation and In vivo Study
Authors: Juniar Kalpika Resmi, Safira Prisya Dewi and Heni RachmawatiAvailable online: 10 December 2024More LessBackgroundBacterial nanocellulose (BNC) is typically produced through fermentation using Hestrin Schramm (HS) médium. However, its high cost limits its use in industry. Moreover, curcumin, as a model substance, is a potential bioactive compound but has low bioavailability. This also limits its use for clinical application. Thus, a delivery system using more affordable production of BNC was develop to improve the lack property of curcumin, focusing on topical route.
ObjectiveThis study aims to determine the best substrate component according to yield value and evaluate the physical properties as well as the permeation capability of BNC as a delivery matrix system for curcumin.
MethodsThe optimization of Gluconacetobacter xylinus culture media to produce BNC was conducted using 6 variation substrates consisting of Palmyra sap (PS) and tofu pulp with certain concentrations. Following a nine-day period, the yield of BNC was calculated. The selected BNCs were then impregnated with curcumin-DMSO and curcumin in the form of nanoemulsion (curcumin- NE). Subsequently, the BNCs containing these curcumin forms were characterized. In vitro testing of curcumin reléased from BNC was conducted using Franz difusión cells. In addition, the penetration ability of curcumin across the mice skin was observed using confocal microscopy. In vivo testing was also conducted to ascertain the safety of BNC-loaded curcumin on mice skin.
ResultsPS-TP substrate (100:0, S-6) was the most appropriate substrate for BNC production, yielding 118.5±0.09 g/L. CR-DMSO and CR-NE were successfully impregnated into BNC. Confocal data showed that both formulations were able to penétrate the dermis layer. There was no significant difference was observed between the administration of BNC/CR-DMSO and BNC/CR-NE against the control.
ConclusionBNC successfully produced using palmyra sap shows promising biomembrane for topical delivery of curcumin. No evidence inflammation or neovascularization in BNC/CR-DMSO- and BNC/CR-NE-treated mice confirms the safety use of this biomembrane.
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Emerging Trends in Transdermal Drug Delivery: Nanoparticle Formulations and Technologies for Enhanced Skin Penetration and Drug Efficiency
By Kiran DudhatAvailable online: 10 December 2024More LessTransdermal drug delivery systems (TDDS) have emerged as a popular non-invasive approach for treating skin-related disorders, offering quick and reliable drug delivery into the skin, thereby accelerating therapeutic efficacy. In India, there is a growing interest in TDDS due to its perceived safety and effectiveness. Researchers are actively developing new formulations and technologies to enhance drug delivery efficiency and reduce side effects. Recent trends indicate a focus on overcoming challenges such as low permeability and stability issues through innovative nanoparticle-based delivery systems. Nanotechnology has revolutionized transdermal drug delivery by offering precise control over nanoparticle properties, enabling enhanced skin permeation and targeted delivery. Various nanoparticle formulations, including polymeric nanoparticles, liposomes, nanotubes, solid lipid nanoparticles, and nanoemulsions, have shown promise in improving drug solubility, bioavailability, and sustained release. Additionally, microneedles have emerged as a successful transdermal delivery method, offering advantages over traditional creams and patches. Metallic nanocarriers and nanoemulsions are also being explored for their potential in targeted drug delivery and enhanced skin penetration. Despite these advancements, challenges such as toxicity and biocompatibility need to be addressed for widespread clinical translation. Overall, the growing interest in transdermal drug delivery systems in India reflects the potential for improved therapeutic outcomes and patient convenience through innovative nanoparticle-based formulations and technologies.
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Empowering Arthritis Patients: Optimized Drug Delivery through Piroxicam Microcapsule-Embedded Scaffold Implants via Box-Behnken Experimental Design
Authors: Sampath Kumar and Mothilal MohanAvailable online: 10 December 2024More LessBackgroundThe necessity for extended drug discharge to alleviate pain without adverse effects underscores the importance of innovative drug delivery systems. Achieving sustained pain relief without compromising patient safety is a critical objective in healthcare. By extending the duration of drug action while suppressing side effects, such systems offer enhanced therapeutic outcomes and improved patient quality of life.
ObjectiveThis study endeavors to develop and appraise an innovative implantable drug delivery system by integrating NSAID-loaded gelatin microcapsules into a gelatin scaffold designed to augment drug delivery efficiency and sustain drug release.
MethodPiroxicam-loaded microcapsules with a 1:1 ratio of poly lactic acid and poly lacto glycolic acid showed smaller particle size, good yield, entrapment efficiency, and discharge. They were selected to make gelatin scaffolds with Box Behnken Design using Design Expert software for optimization. The better scaffolds were made in the form of rod-shaped sub-dermal implants. The primary focus of the investigation was the evaluation of critical parameters, specifically entrapment efficiency and drug discharge properties as dependent variables.
ResultsMicrocapsules with a 1:1 ratio of PLA and PLGA showed smaller particle sizes, good yield, entrapment efficiency, and discharge. Notably, the Design Expert-driven optimization yields highly favorable results. Furthermore, the scaffolds loaded with microcapsules exhibited favorable physicochemical assets, including drug discharge, for an extended period, underscoring their versatility for drug delivery.
ConclusionBy employing Design Expert software for optimization, the study demonstrates promising results, particularly in sustained pain management for arthritis, potentially improving therapeutic outcomes and patient quality of life. The study concludes that the prepared implants (holding scaffolds impregnated with piroxicam-loaded microcapsules) can be promising for relieving arthritis all day.
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A Biodegradable and Biocompatible Dental Hemostatic Gelatin Sponge Containing Aloe Vera Nanoparticles; Investigation in Rat Animal Model
Available online: 10 December 2024More LessIntroductionA variety of hemostatic materials have been provided to accelerate the blood clotting process in dentistry. The purpose of this study was to investigate the biocompatibility and biodegradability of a hemostatic dental sponge containing aloe vera nanoparticles in rat animal models.
Methods and MaterialsTwelve adult Wistar rats in the weight range of 200 ± 30 grams and the same age range were randomly divided into two groups of test and control, and each group was divided into three subgroups of 3 days, 7 days, and 14 days. For implantation of the sponge, the animals were anesthetized with xylazine and ketamine, and a piece of the sponge was implanted under the skin at the cut site. In the control group of rats, only the skin was cut and sutured. After the specified number of days, the rats were anesthetized, and in addition to blood sampling, a tissue sample was taken from the animal's surgical site and fixed in 10% formalin. Then the samples were examined in macroscopic and microscopic conditions and finally, the obtained data were statistically analyzed.
ResultsThe results obtained in the present study indicated that the hemostat sponge had no side effects (biocompatible). In addition, it was completely absorbed during the 14 days of the study (biodegradable).
ConclusionAccording to the characteristics of biocompatibility and biodegradability, the studied sponge can be used to control bleeding during dental surgeries or tooth extraction.
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Silk Fibroin Hydrogels: Cutting-Edge Developments and Future Directions
Available online: 10 December 2024More LessThe exploration of hydrogel materials has gained significant attention due to the ongoing period of collaborative interdisciplinary advancements. Silk fibroin (SF) possesses remarkable attributes, such as less immunogenicity, sterilization efficacy, processability without chemical crosslinkers, excellent biocompatibility, low immunogenicity, non-toxicity, mechanical strength, thermal stability, non-carcinogenicity, and adjustable biodegradability make it a highly valuable biomaterial. Silk fibroin hydrogel (SFH), a versatile biomaterial, has garnered significant attention due to its unique properties. Its biocompatibility, tunable mechanical properties, water retention capacity, and bioactive nature offer a unique combination of features that can effectively promote tissue regeneration and enhance wound healing. The utilization of SF for hydrogel production presents a valuable opportunity to leverage natural resources and promote eco-friendly production practices. With their exceptional properties and versatile applications in biomedicine, silk protein-based hydrogels hold promise for various research fields. This review aims to discuss the potential properties and recent advancements in the application of SF-based hydrogels for preclinical skin wound healing.
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Formulation and Assessment of an Optimized Glimepiride Transdermal Therapeutic System Using 32 Full Factorial Design Approach
Authors: Audumbar Mali and Sunayana MaliAvailable online: 10 December 2024More LessBackgroundCurrently, a large number of populations are suffering from diabetes mellitus, which significantly increases the burden on public health. Glimepiride is an antidiabetic drug with a shorter half-life (approximately 5 hours), low bioavailability, and first-pass metabolism. Due to these limitations, it is required to maintain a uniform therapeutic level, and it has been chosen as a transdermal drug delivery approach.
ObjectivesThe main objective of this investigation was to evaluate glimepiride-loaded transdermal patches on the skin to treat diabetes mellitus. To overcome the issue of oral glimepiride and provide a localized effect, a transdermal drug delivery approach was developed.
MethodsThe glimepiride transdermal drug delivery approach was developed by using the solvent evaporation method. To examine the impact of altering amounts of polyvinyl alcohol (X1) and polyvinyl pyrrolidone (X2) on tensile strength, % of glimepiride released in 12 hours (Q12), and % of glimepiride released in 24 hours (Q24), as reliant on variables, a 32 complete factorial design was employed. For dependent variables, regression estimation and estimation of variance were employed. In-vitro release statistics were fixed to different models for various glimepiride release kinetics. In-vitro glimepiride release was tested using the best formulation.
ResultsThe formulation F4 with 1300.00 milligrams of polyvinyl alcohol and 600.00 milligrams of polyvinyl pyrrolidone demonstrated a release of 96.17% for up to 24 hours and zero order release kinetics consisting of r2=0.987, which was the best batch. The optimized formulation F4 showed a controlled release of glimepiride and better permeation and deposition properties.
ConclusionThe findings of this research work demonstrated the potential of the 32 full factorial mathematical models created to anticipate formulations with additional desirable release and permeability qualities for the treatment of diabetes mellitus.
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A Review on Silver Nanoparticles: Synthesis Approaches, Properties, Characterization and Applications
Authors: CK Vishveshwaraiah, GB Kirankumar, M Harshitha and BK MadhuAvailable online: 01 November 2024More LessNanoparticles are a significant topic due to their applications in various fields, including biology, optics, catalysis, pharmaceutics, health, agriculture, and industry, with biosynthesis processes being quick, easy, and environmentally friendly. Due to their applications across multiple industries, silver nanoparticles, or AgNPs, have become the most desired nanoparticles with the recent development of nanotechnology. The physical, chemical, and biological characteristics of AgNPs are being studied. These characteristics are crucial for limiting the hazards associated with silver nanoparticles while optimizing their potential applications in many fields. A higher degree of toxicity in both the environment and living things could arise from the increasing use of silver nanoparticles in the product. Silver nanoparticles find application in wound care, anti-infective therapy, food, pharmaceutical, and cosmetic industries. As antioxidant, antiviral, anticancer, antifungal, anti-inflammatory, and microbiological agents, silver nanoparticles are widely used. Not only must the particles be nanoscale in order for silver nanoparticles to be present, but their production must also be simple and inexpensive to achieve. This paper aims to review the different methods of synthesis of silver nanoparticles, properties, characterization, and their applications. In specific, several chemical and green synthesis approaches for synthesising silver nanoparticles have been discussed. The morphology, size, thermal properties, toxicity properties, electrical properties, catalytic properties, and applications of silver nanoparticles are focused. The main focus is on the effective and efficient synthesis of pure silver nanoparticles and their potential applications.
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A Comprehensive Review on Oleic Acid Vesicles: A Novel Approach to Drug Delivery
Authors: S Sandhya, Jayatheertha S Lokapur and Prakash S GoudanavarAvailable online: 24 October 2024More LessThe implementation of several innovative drug delivery technologies has made medication distribution more focused and managed in recent years. These days, a vesicular drug delivery system defines the rate of distribution and the site of action in order to improve the action and increase patient compliance; there are various kinds of newly developed vesicular drug delivery systems, including transferosomes, niosomes, aquasomes, ufasomes, pharmacosomes, and phytosomes. Ufasomes are unsaturated fatty acid vesicles with a limited pH range of 7 to 9. They are a suspension of closed lipid bilayers made of fatty acids and their ionized species. The hydrocarbon tails of fatty acid molecules are oriented toward the membrane's inner core, and their carboxyl groups are in contact with water. The two fatty acids that are most frequently employed in the ufasomes’ manufacturing process are oleic and linoleic acids. It is a common practice to produce fatty acid vesicles via the thin film hydration process. The manufacture of stable ufasomes is mostly dependent on the choice of fatty acids, amount of cholesterol, pH range, buffer, etc. This article goes into additional detail regarding unsaturated fatty acids’ characteristics, benefits, and drawbacks.
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Chromatography and Spectroscopic Technique-Based Rapid Characterization of Nano-Carrier Pharmaceuticals
Authors: Shamim1* and Tarmeen AliAvailable online: 21 October 2024More LessA nanocarrier is a novel colloidal system whose particle size ranges between 1-100 nm. It is extensively utilized in drug delivery and various other sectors, such as the pharmaceutical, food, and dairy industries. The nanocarrier systems, including solid lipid nanoparticles, micelles, liposomes, and other encapsulated compounds, have improved stability, solubility, bioavailability, and quality. Nanocarriers offer therapeutic effectiveness with low toxicity because of their biocompatibility and ability to cross body barriers. Various analytical techniques, such as chromatography and spectroscopy, are crucial in qualitative and quantitative analysis of nanocarrier-based formulations. Molecular identification and drug content determination require chromatographic techniques, particularly HPLC. Spectroscopic techniques such as LC-MS, NMR, GC-MS, CE-MS, Raman, and IR are used to analyze the interaction and molecular structure of the sample. Nanocarriers have several benefits but face various challenges like stability, drug loading, regulatory standards, and biocompatibility. Future surface engineering and nanocarrier design advancements could improve targeted drug delivery and sustained diagnostic applications, significantly impacting healthcare.
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A Comprehensive Review on the Self-Nanoemulsifying System for the Delivery of Herbal Drugs
Authors: Manoj Harde and Rashmi MallyaAvailable online: 11 October 2024More LessSelf-Nanoemulsifying Drug Delivery Systems (SNEDDSs) are an isotropic mixture of oils, co-surfactants, and surfactants and can form fine O/W nanoemulsions in aqueous media. These components are advantageous in terms of improved solubility and bioavailability, as limited permeability, solubility, and bioavailability remain a significant challenge in the development of herbal drugs. This review explores the potential of self-nanoemulsifying drug delivery systems (SNEDDSs) as a promising strategy to overcome this problem. The SNEDDSs are considered to be a novel technique for the delivery of low water-soluble drugs. They can bypass the first-pass metabolism, which ultimately results in steady and sustained drug levels in the systemic circulation. The present article provides a comprehensive overview of the SNEDDSs formulation of herbal drugs. It includes their composition, characterization, in vitro and in vivo studies conducted on various disease conditions, and their pharmacokinetic studies.
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Lipid-Based Nanoparticles as Drug Delivery System for Modern Therapeutics
Authors: Shivani Gandhi and Divyesh Harshadkumar ShastriAvailable online: 11 October 2024More LessThe emergence of lipid-based nanoparticulate systems has significantly reshaped the landscape of drug delivery. This review aims to encapsulate the advancements, challenges, and potential of lipid-based nanoparticulate drug delivery in modern therapeutics. Lipid-based nanoparticles, including liposomes, lipid nanoparticles, and solid lipid nanoparticles, harness the biocompatibility and biodegradability of lipids to encapsulate and deliver a diverse range of therapeutic agents. This platform offers solutions to various drug delivery challenges, such as enhancing drug solubility and bio- availability, achieving controlled and sustained release, targeted delivery, and co-delivery of multi-agents. These nanoparticles have demonstrated potential in overcoming biological barriers, including the blood-brain barrier, mucosal barriers, and cellular barriers, enabling the delivery of drugs to previously inaccessible sites. Biocompatibility and reduced toxicity are intrinsic attributes of lipid-based nanoparticles, minimizing immune responses and systemic toxicity while promoting personalized medicine possibilities. However, challenges in formulation, stability, and regulatory approval underscore the need for ongoing research and innovation in this field.
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Copper Nanoparticles: Characterization, Synthesis, and Biological Activity – A Review
Available online: 09 October 2024More LessCopper and copper-based nanoparticles, derived from the abundant and cost-effective copper metal, have garnered significant attention due to their unique properties and potential for various applications. Copper is a biogenic metal that is found in all kingdoms of life and has a variety of essential biological activities. Among the earliest metals that humanity has harvested and exploited, copper has played a crucial role in maintaining and advancing civilization since the beginning of time. The article provided sources that shed light on the synthesis, characteristics, and applications of copper and copper nanoparticles, highlighting their historical significance and diverse range of uses.
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The Beauty Revolution of Nanotechnology: Unveiling the Impact of Cosmetic Nano Wonders
Authors: Parul Gupta, Anjali Sharma and Vishnu MittalAvailable online: 08 October 2024More LessThe infusion of nanotechnology into cosmetic formulations marks a transformative shift in beauty science. Although Raymond Reed originally used the word “cosmeceutical,” Dr. Albert Kligman popularised the idea in the late 1970s. Cosmetic Nano Wonders are redefining skincare by leveraging nanomaterials to enhance the stability, delivery, and efficacy of active ingredients. The paradigm shift holds promise for overcoming longstanding challenges in traditional cosmetic formulations. This article aims to explore and showcase the revolutionary impact of nanotechnology on the cosmetic industry. Focusing on key nanocarriers, such as liposomes and nanoparticles, our objective is to illuminate how nanotechnology elevates the performance of beauty products, providing advanced solutions for skincare concerns. This revolution promotes sustainability through green synthesis techniques and enables more accurate and effective therapies for a variety of skin issues, including acne and ageing that raises the bar for safety and innovation in the cosmetics business by enhancing product performance and environmental impact. Conducting a thorough literature review, we analyze recent scientific studies and industry reports to unveil the mechanisms and applications of nanotechnology in cosmetics. Special attention is given to the role of nanocarriers in stability enhancement, targeted delivery, and controlled release, unraveling the methods that drive the transformative potential of Cosmetic Nano Wonders. The database sources are Scopus, PubMed, Google Scholar, and Google Patents. The examination of recent research underscores the tangible benefits of nanotechnology in cosmetics. Cosmetic Nano Wonders demonstrate superior stability, enhanced penetration into skin layers, and controlled release mechanisms, showcasing their potential to revolutionize beauty science and address longstanding challenges in skincare. Cosmetic Nano Wonders represent a groundbreaking shift in beauty science, offering unprecedented possibilities for formulators and consumers. As nanotechnology continues to reshape cosmetic formulations, the future holds the promise of safer, more effective, and personalized skincare solutions, ushering in a new era in beauty science.
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Nanocurcumin-containing Spongy Membrane for Improving the Quality of Hard and Soft Tissues in the Extracted Tooth Area: A Double-Blind Split-Mouth Clinical Trial Study
Available online: 30 August 2024More LessBackgroundThe assessment of the hard and soft tissue conditions is part of the overall dental treatments.
AimIn this study, we investigated nano curcumin-containing membranes to improve the quality of the hard and soft tissues in the extracted tooth area as a clinical trial study.
MethodsAfter the patient was selected following the inclusion and exclusion criteria, the patients who had teeth extracted from both sides of the mouth (split mouth) on the side of the intervention received a membrane containing nanocurcumin, and on the control side, no material was placed in the socket. For data analysis, SPSS software version 24 was used. A significance threshold was deemed to be less than 0.05 in terms of probability.
ResultsTwo months after tooth extraction, during implant placement, the average gingival thickness on the “intervention side,” was 3.1±0.34 mm, while the average gingival thickness on the “control side” was 2.6±0.42 mm. Then, the membrane could improve the quality of soft tissue (P< 0.0001). As another outcome, the application of this membrane did not significantly affect bone repair in these patients compared to the control group (P = 0.72). However, the histology data revealed that the newly generated bone of the intervention group was seen close to the membrane, demonstrating the osteoconductive ability of the membrane.
ConclusionBased on the obtained results, the newly developed membrane can be used to improve the quality of hard and soft tissues in the extracted tooth area. Nonetheless, more efforts in nanocurcumin dosage adjustment are needed for hard tissue regeneration in future studies.
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