Smart Lipid-Based Nanosystems for Therapeutic Immune Induction against Cancers: Perspectives and Outlooks

Cancer immunotherapy, a promising and widely applied mode of oncotherapy, makes use of immune stimulants and modulators to overcome the immune dysregulation present in cancer, and leverage the host’s immune capacity to eliminate tumors. Although some success has been seen in this field, toxicity and weak immune induction remain challenges. Liposomal nanosystems, previously used as targeting agents, are increasingly functioning as immunotherapeutic vehicles, with potential for delivery of contents, immune induction, and synergistic drug packaging. These systems are tailorable, multifunctional, and smart. Liposomes may deliver various immune reagents including cytokines, specific T-cell receptors, antibody fragments, and immune checkpoint inhibitors, and also present a promising platform upon which personalized medicine approaches can be built, especially with preclinical and clinical potentials of liposomes often being frustrated by inter- and intrapatient variation. In this review, we show the potential of liposomes in cancer immunotherapy, as well as the methods for synthesis and in vivo progression thereof. Both preclinical and clinical studies are included to comprehensively illuminate prospects and challenges for future research and application.

Laser Transmission Welding of Aluminum Film Coated With Heat Sealable Co-Polyester Resin With Polypropylene Films For Applications In Food & Drug Packaging

The present work deals with the high-power diode laser joining process of aluminum films coated with a polyester resin with polypropylene (PP) films. The first part of the work focused on analyzing the coating process of aluminum films with a polyester resin, using an automatic applicator. The second part of the work was focused on the analysis of the laser joining process of coated aluminum films with plastic counterparts made of PP. Different thicknesses and colors of the PP parts were tested in order to analyze the joining process under a wide range of different conditions. The experimental plan involved the study of the influence of the laser joining parameters, in particular the scanning speed and beam power, on the joints. The joints between aluminum and PP films were subsequently tested by means of tensile and peel-off tests. The results allowed the detection of the best processing conditions, stating the high potential of laser systems in the joining process of aluminum and PP films for food packaging applications.

Drug Packaging Management Based on the Effect of Medical Images on the Intracellular Polysaccharide Synthesis and Antivertigo Activity of Phalaenopsis

Many clinically important drugs come directly or indirectly from higher plants. People are increasingly aware of the role of the human immune system in maintaining good health. Diseases related to physical dysfunction, such as vertigo, have attracted increasing attention from medical researchers and clinicians. In this paper, some compounds isolated and identified from medicinal fomes showed promising antivertigo properties. Medical images were used to classify and synthesize polysaccharides in the management of drug subpackages of Cladosporium intracellular polysaccharides. The scientific explanation of how these compounds work in animal and human systems is increasing exponentially. Studies have found that all of these compounds can enhance the innate and adaptive immune responses of the host and activate various immune cells that are important for maintaining homeostasis, such as host cells and chemical messengers, triggering complement and acute phase reactions. The antivertigo compounds derived from the intracellular polysaccharides of Phellinus mucronatus had an activity interference of 35% without drug subpackage. Although the antivertigo activity of many intracellular polysaccharides from Fovea xylostella can reach 86%, only a few of them have been proved to have antivertigo activity. In addition, they can be considered as multicytokine inducers that can induce the expression of various immune-regulatory cytokines and cytokine receptor genes. Lymphocytes that control antibody production and cell-mediated cytotoxicity are also stimulated.

An Early Warning Monitoring System for Illicit Drug Use at Large Public Events: ‘Close to Real Time’ Trace Residue Analysis of Discarded Drug Packaging Samples

Inspired by the exchange principle espoused by Edmond Locard (1877-1966), which states “every contact leaves a trace”, we report here the development and application of a strategy for trace residue sampling and analysis of discarded ‘Drug Packaging Samples’ (DPS), as part of an early warning monitoring system for illicit drug use at large public events. Using Direct Analysis in Real Time (DART) - mass spectrometry (MS) and -tandem mass<br>spectrometry (MS/MS), rapid and high-throughput identification and characterisation of a wide range of illicit drugs and adulterant substances was achieved, including those present in complex poly-drug mixtures and at low relative abundances, and with analysis times of less than one minute per sample. 1362 DPS were analysed either ‘off-site’ using laboratory-based instrumentation or in ‘on-site’ in ‘close to real time’ using a transportable mass spectrometer housed within a customised mobile analytical laboratory. 92.2% of DPS yielded positive results for at least one of 15 different pharmacologically active drugs and/or adulterants, including cocaine, MDMA, and ketamine, as well as numerous ‘novel psychoactive substances’ (NPS). Notably, polydrug mixtures were more common than single drugs, with 52.6% of positive DPS found to contain more than one substance, and with 42 different drug and polydrug combinations observed throughout the study. For analyses performed ‘on-site’, reports to key stakeholders including event organisers, first aid and medical personnel, and peer-based harm reduction workers could be provided in as little as 5 minutes after sample collection. Then, following risk assessment of the potential harms associated with their use, drug advisories or alerts were then disseminated to event staff and patrons, and subsequently to the general public, when substances with particularly toxic properties were identified.<br>

An Early Warning Monitoring System for Illicit Drug Use at Large Public Events: ‘Close to Real Time’ Trace Residue Analysis of Discarded Drug Packaging Samples

Inspired by the exchange principle espoused by Edmond Locard (1877-1966), which states “every contact leaves a trace”, we report here the development and application of a strategy for trace residue sampling and analysis of discarded ‘Drug Packaging Samples’ (DPS), as part of an early warning monitoring system for illicit drug use at large public events. Using Direct Analysis in Real Time (DART) - mass spectrometry (MS) and -tandem mass<br>spectrometry (MS/MS), rapid and high-throughput identification and characterisation of a wide range of illicit drugs and adulterant substances was achieved, including those present in complex poly-drug mixtures and at low relative abundances, and with analysis times of less than one minute per sample. 1362 DPS were analysed either ‘off-site’ using laboratory-based instrumentation or in ‘on-site’ in ‘close to real time’ using a transportable mass spectrometer housed within a customised mobile analytical laboratory. 92.2% of DPS yielded positive results for at least one of 15 different pharmacologically active drugs and/or adulterants, including cocaine, MDMA, and ketamine, as well as numerous ‘novel psychoactive substances’ (NPS). Notably, polydrug mixtures were more common than single drugs, with 52.6% of positive DPS found to contain more than one substance, and with 42 different drug and polydrug combinations observed throughout the study. For analyses performed ‘on-site’, reports to key stakeholders including event organisers, first aid and medical personnel, and peer-based harm reduction workers could be provided in as little as 5 minutes after sample collection. Then, following risk assessment of the potential harms associated with their use, drug advisories or alerts were then disseminated to event staff and patrons, and subsequently to the general public, when substances with particularly toxic properties were identified.<br>

Dispensing errors in hospital pharmacies: A prospective study in Yemen

AimsThe aim of this study was to describe the dispensing errors that occurred during the dispensing process in selected hospital pharmacies in Sana’a, Yemen; and to describe their types and causes.MethodologyA prospective study was carried out in selected hospital pharmacies in Yemen over 40 days using a validated tool. ResultsA total of 9000 dispensed prescriptions were evaluated for the dispensing errors and 2.13 % dispensing errors were identified. Wrong dosage form (134/192); wrong strength (24/192); wrong drug (18/192); wrong quantity, wrong instructions written and drug available in the pharmacy but not given were (6/192) and dispense the expired drugs (3/192) were the reported dispensing errors in this study. Poor handwriting, similar drug names, similar drug packaging, fatigue, heavy work, workforce issues, and poor communication were the most common reported causes of dispensing errors. ConclusionThe prevalence of dispensing errors in this study was 2.13%. Pharmacists can play an important role in the improving the safety of medicines. Study of the dispensing errors incidence in national wide, it's types and causes of dispensing errors are very important and highly recommended. Study the impact of different interventions to improve dispensing quality, reducing and preventing dispensing errors are strongly recommended.

Pharmacokinetic Research Progress of Anti-tumor Drugs Targeting for Pulmonary Administration

Background:: Cancer is a major problem that threatens human survival and has a high mortality rate. The traditional chemotherapy methods are mainly intravenous injection and oral administration, but have obvious toxic and side effects. Anti-tumor drugs for pulmonary administration can enhance drug targeting, increase local drug concentration, and reduce the damage to systemic organs, especially for the treatment of lung cancer. Methods:: The articles on the pharmacokinetics of anti-tumor drugs targeting pulmonary administration were retrieved from the Pub Med database. This article mainly took lung cancer as an example and summarized the pharmacokinetic characteristics of anti-tumor drugs targeting for pulmonary administration contained in nanoparticles, dendrimers, liposomes and micelles. Results:: The review shows that the pharmacokinetics process of pulmonary administration is associated with a drug carrier by increasing the deposition and release of drugs in the lung, and retarding the lung clearance rate. Among them, the surface of dendrimers could be readily modified, and polymer micelles have favorable loading efficiency. In the case of inhalation administration, liposomes exhibit more excellent lung retention properties compared to other non-lipid carriers. Therefore, the appropriate drug carrier is instrumental to increase the curative effect of anti-tumor drugs and reduce the toxic effect on surrounding healthy tissues or organs. Conclusion:: In the process of pulmonary administration, the carrier-embedded antitumor drugs have the characteristics of targeted and sustained release compared with non-packaging drugs, which provides a theoretical basis for the clinical rational formulation of chemotherapy regimens. However, there is currently a lack of comparative research between drug packaging materials, and more importantly, the development of safe and effective anti-tumor drugs targeting for pulmonary administration requires more data.