COVID-19 test could technically be nasal vaccine
The vigilant are aware of DNA-modification capabilities of the COVID-19 mRNA-vaccines.
The distrusting deem it plausible nanorobotics, via hydrogel or otherwise, could be in the vaccine.
Doctor Carrie Madej voiced her concerns publicly after finding out that information.
The research in the picture is in the public domain and describes how nasal swabs used for covid testing, could be used to incorporate the fore-mentioned concerns.
Research papers explain how nasal swabs can be used for vaccination.
Research paper sources
Johns Hopkins developed Theragrippers for nasal drug delivery
IN EGYPT THIS WAS A PUNISHMENT FOR SLAVES. EXPOSED ! NANOTECHNOLOGY IN THE COVID-19 SWABS TEST ! Swab sounds like Klaus “Schwab”
Do not take the Covid 19 test. It can change your DNA and is one of the Marks of the Beast. The Beast has more than one Mark. The Covid swab test has nanobot technology on it that can change your DNA and harm you and give you a virus or worse.
A 5G whistleblower warned us that this was the psychopath’s plans all along. See link below.
MAX IGAN NAILS THE SWAB TEST AS A POSSIBLE REASON WHY PEOPLE GET SICK AFTER HAVING ONE [SHORT CLIP]
MIRROR SOURCE: (I made a small clip from Max’s recent video to pin down the swab test being a attack vector).
THE COMING ZOMBIE APOCALYPSE – The Crowhouse
The Covid-19 test is another form of the Mark of the Beast as it can change and corrupt our DNA.
Find out why the Covid 19 test has to go all the way to your brainstem. Are you they checking to see if you have a brain? Find out now.
DR. LORRAINE DAY WARNS PEOPLE OF WHAT’S COMING
Dr. Lorraine Day interviewed by Jana Bennun of Israeli News LIVE. Dr. Lorraine Day is one of the most fearless truth-tellers alive. Topics include the CV19 fraud, the patenting of CV19 and the coming patenting of human beings, staying healthy, vaccines and the coming CV19 injections, genocide of the white & Christian population (The Tribes of Jacob-Israel), satanic influence in the Agenda being imposed upon the world, historical interpretation of King Jesus’ life, the re-writing of the Bible to make the Edomite Jews the chosen people in order to serve the Edomite Jewish agenda of world dominaiton, and much more!
It is well known that the Covid-19 tests are contaminated and people should not be taking the Covid-19 test as it could damage / corrupt your DNA and cause you permanent physical harm. The CDC even confirmed that the Covid-19 tests kits were contaminated in April 2020. The only way to catch a virus is to be injected with it through the Covid-19 tests and Covid-19 vaccines.
The Coivd-19 vaccine and the Covid-19 Test are both Marks of the Beast as they both change the DNA. The Beast has more than one Mark. Elon Musk’s neuralink is another Mark of the Beast. We are supposed to keep our DNA pure and God of Abraham Isaac and Jacob’s Holy spirit will not dwell in us if we change our DNA and become a transhuman or a machine or corrupt our DNA.
DR. LORRAINE DAY: YOU’VE ALREADY BEEN VACCINATED WHEN YOU TOOK SWAB TEST
DR. LORRAINE DAY QUOTES AND FURTHER EXPLAINS OUR REPORT ON TEST SWABS AND NANOTECH
This is what she’s quoting: https://silview.media/2020/11/26/they-can-vaccinate-us-through-nasal-test-swabs/
The Covid-19 test is another form of the Mark of the Beast as it can change and corrupt our DNA. See Dr. Lorraine Day’s interview with Jana link below. The Covid-19 vaccine and the Neuralink are also Marks of the Beast. The Devil has more than one Mark of the Beast Do not insert anything into your body such as the Covid-19 test or Covid-19 vaccine or any vaccine or affix anything to your body such as electronics and tattoos. Anything that changes or corrupts your DNA is a Mark of the Beast!
CDC’s failed coronavirus tests were tainted with coronavirus, feds confirm
posted by Weaver
by Silviu “Silview” Costinescu_
I don’t know if they do it, because no independent researchers examine those swabs, but I have always pointed out that our overlords seem more concerned with testing than with vaccinating. Almost like the vaccines were the bait and tests were the switch. And now we also know they totally CAN do that. Just follow the science below.
November 3, 2020
RESEARCHERS ENGINEER TINY MACHINES THAT DELIVER MEDICINE EFFICIENTLY
A theragripper is about the size of a speck of dust. This swab contains dozens of the tiny devices. Credit: Johns Hopkins University.
Inspired by a parasitic worm that digs its sharp teeth into its host’s intestines, Johns Hopkins researchers have designed tiny, star-shaped microdevices that can latch onto intestinal mucosa and release drugs into the body.
David Gracias, Ph.D., a professor in the Johns Hopkins University Whiting School of Engineering, and Johns Hopkins gastroenterologist Florin M. Selaru, M.D., director of the Johns Hopkins Inflammatory Bowel Disease Center, led a team of researchers and biomedical engineers that designed and tested shape-changing microdevices that mimic the way the parasitic hookworm affixes itself to an organism’s intestines.
Made of metal and thin, shape-changing film and coated in a heat-sensitive paraffin wax, “theragrippers,” each roughly the size of a dust speck, potentially can carry any drug and release it gradually into the body.
The team published results of an animal study this week as the cover article in the journal Science Advances.
Gradual or extended release of a drug is a long-sought goal in medicine. Selaru explains that a problem with extended-release drugs is they often make their way entirely through the gastrointestinal tract before they’ve finished dispensing their medication.
“Normal constriction and relaxation of GI tract muscles make it impossible for extended-release drugs to stay in the intestine long enough for the patient to receive the full dose,” says Selaru, who has collaborated with Gracias for more than 10 years. “We’ve been working to solve this problem by designing these small drug carriers that can autonomously latch onto the intestinal mucosa and keep the drug load inside the GI tract for a desired duration of time.”
When an open theragripper, left, is exposed to internal body temperatures, it closes on the instestinal wall. In the gripper’s center is a space for a small dose of a drug. Credit: Johns Hopkins University
Thousands of theragrippers can be deployed in the GI tract. When the paraffin wax coating on the grippers reaches the temperature inside the body, the devices close autonomously and clamp onto the colonic wall. The closing action causes the tiny, six-pointed devices to dig into the mucosa and remain attached to the colon, where they are retained and release their medicine payloads gradually into the body. Eventually, the theragrippers lose their hold on the tissue and are cleared from the intestine via normal gastrointestinal muscular function.
Taken from the original research annexes
Gracias notes advances in the field of biomedical engineering in recent years.
“We have seen the introduction of dynamic, microfabricated smart devices that can be controlled by electrical or chemical signals,” he says. “But these grippers are so small that batteries, antennas and other components will not fit on them.”
Theragrippers, says Gracias, don’t rely on electricity, wireless signals or external controls. “Instead, they operate like small, compressed springs with a temperature-triggered coating on the devices that releases the stored energy autonomously at body temperature.”
The Johns Hopkins researchers fabricated the devices with about 6,000 theragrippers per 3-inch silicon wafer. In their animal experiments, they loaded a pain-relieving drug onto the grippers. The researchers’ studies found that the animals into which theragrippers were administered had higher concentrates of the pain reliever in their bloodstreams than did the control group. The drug stayed in the test subjects’ systems for nearly 12 hours versus two hours in the control group.
“Swarms of microscopic robots that can be injected” Tell Melinda Gates we can inject robots these days.
Shadab Md 1 , Gulam Mustafa 2 3 , Sanjula Baboota 3 , Javed Ali 3 Affiliations Expand
Context: Brain disorders remain the world’s leading cause of disability, and account for more hospitalizations and prolonged care than almost all other diseases combined. The majority of drugs, proteins and peptides do not readily permeate into brain due to the presence of the blood-brain barrier (BBB), thus impeding treatment of these conditions.
Objective: Attention has turned to developing novel and effective delivery systems to provide good bioavailability in the brain.
Methods: Intranasal administration is a non-invasive method of drug delivery that may bypass the BBB, allowing therapeutic substances direct access to the brain. However, intranasal administration produces quite low drug concentrations in the brain due limited nasal mucosal permeability and the harsh nasal cavity environment. Pre-clinical studies using encapsulation of drugs in nanoparticulate systems improved the nose to brain targeting and bioavailability in brain. However, the toxic effects of nanoparticles on brain function are unknown.
Result and conclusion: This review highlights the understanding of several brain diseases and the important pathophysiological mechanisms involved. The review discusses the role of nanotherapeutics in treating brain disorders via nose to brain delivery, the mechanisms of drug absorption across nasal mucosa to the brain, strategies to overcome the blood brain barrier, nanoformulation strategies for enhanced brain targeting via nasal route and neurotoxicity issues of nanoparticles.
Epub 2013 Oct 16.
NANOEMULSION-BASED INTRANASAL DRUG DELIVERY SYSTEM OF SAQUINAVIR MESYLATE FOR BRAIN TARGETING
Hitendra S Mahajan 1 , Milind S Mahajan, Pankaj P Nerkar, Anshuman Agrawal Affiliations Expand
The central nervous system (CNS) is an immunological privileged sanctuary site-providing reservoir for HIV-1 virus. Current anti-HIV drugs, although effective in reducing plasma viral levels, cannot eradicate the virus completely from the body. The low permeability of anti-HIV drugs across the blood-brain barrier (BBB) leads to insufficient delivery. Therefore, developing a novel approaches enhancing the CNS delivery of anti-HIV drugs are required for the treatment of neuro-AIDS. The aim of this study was to develop intranasal nanoemulsion (NE) for enhanced bioavailability and CNS targeting of saquinavir mesylate (SQVM). SQVM is a protease inhibitor which is a poorly soluble drug widely used as antiretroviral drug, with oral bioavailability is about 4%. The spontaneous emulsification method was used to prepare drug-loaded o/w nanoemulsion, which was characterized by droplet size, zeta potential, pH, drug content. Moreover, ex-vivo permeation studies were performed using sheep nasal mucosa. The optimized NE showed a significant increase in drug permeation rate compared to the plain drug suspension (PDS). Cilia toxicity study on sheep nasal mucosa showed no significant adverse effect of SQVM-loaded NE. Results of in vivo biodistribution studies show higher drug concentration in brain after intranasal administration of NE than intravenous delivered PDS. The higher percentage of drug targeting efficiency (% DTE) and nose-to-brain drug direct transport percentage (% DTP) for optimized NE indicated effective CNS targeting of SQVM via intranasal route. Gamma scintigraphy imaging of the rat brain conclusively demonstrated transport of drug in the CNS at larger extent after intranasal administration as NE.
Intranasal nanoemulsion based brain targeting drug delivery system of risperidone. Kumar M, Misra A, Babbar AK, Mishra AK, Mishra P, Pathak K. Int J Pharm. 2008 Jun 24;358(1-2):285-91. doi: 10.1016/j.ijpharm.2008.03.029. Epub 2008 Mar 27. PMID: 18455333
Preliminary brain-targeting studies on intranasal mucoadhesive microemulsions of sumatriptan. Vyas TK, Babbar AK, Sharma RK, Singh S, Misra A. AAPS PharmSciTech. 2006 Jan 20;7(1):E8. doi: 10.1208/pt070108. PMID: 16584167
Nanoneurotherapeutics approach intended for direct nose to brain delivery. Md S, Mustafa G, Baboota S, Ali J. Drug Dev Ind Pharm. 2015;41(12):1922-34. doi: 10.3109/03639045.2015.1052081. Epub 2015 Jun 9. PMID: 26057769 Review.
Intranasal microemulsion for targeted nose to brain delivery in neurocysticercosis: Role of docosahexaenoic acid. Shinde RL, Bharkad GP, Devarajan PV. Eur J Pharm Biopharm. 2015 Oct;96:363-79. doi: 10.1016/j.ejpb.2015.08.008. Epub 2015 Aug 28. PMID: 26318978
Targeted drug delivery to the brain via intranasal nanoemulsion: Available proof of concept and existing challenges. Chatterjee B, Gorain B, Mohananaidu K, Sengupta P, Mandal UK, Choudhury H. Int J Pharm. 2019 Jun 30;565:258-268. doi: 10.1016/j.ijpharm.2019.05.032. Epub 2019 May 13. PMID: 31095983 Review.
HYDROGEL NANOPARTICLES AND NANOCOMPOSITES FOR NASAL DRUG/VACCINE DELIVERY
Sara Salatin 1 2 , Jaleh Barar 1 3 , Mohammad Barzegar-Jalali 3 , Khosro Adibkia 3 4 , Mitra Alami Milani 2 4 , Mitra Jelvehgari 5 6 Affiliations Expand
1 Research Center for Pharmaceutical Nanotechnology, Tabriz University of Medical Science, Tabriz, Iran.
2 Student Research Committee, Tabriz University of Medical Science, Tabriz, Iran.
3 Department of Pharmaceutics, Faculty of Pharmacy, Tabriz University of Medical Sciences, Mailbox 51664, Tabriz, Iran.
4 Drug Applied Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
5 Department of Pharmaceutics, Faculty of Pharmacy, Tabriz University of Medical Sciences, Mailbox 51664, Tabriz, Iran. firstname.lastname@example.org.
6 Drug Applied Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran. email@example.com.
Over the past few years, nasal drug delivery has attracted more and more attentions, and been recognized as the most promising alternative route for the systemic medication of drugs limited to intravenous administration. Many experiments in animal models have shown that nanoscale carriers have the ability to enhance the nasal delivery of peptide/protein drugs and vaccines compared to the conventional drug solution formulations. However, the rapid mucociliary clearance of the drug-loaded nanoparticles can cause a reduction in bioavailability percentage after intranasal administration. Thus, research efforts have considerably been directed towards the development of hydrogel nanosystems which have mucoadhesive properties in order to maximize the residence time, and hence increase the period of contact with the nasal mucosa and enhance the drug absorption. It is most certain that the high viscosity of hydrogel-based nanosystems can efficiently offer this mucoadhesive property. This update review discusses the possible benefits of using hydrogel polymer-based nanoparticles and hydrogel nanocomposites for drug/vaccine delivery through the intranasal administration.
Keywords: Brain; Hydrogel; Nanoparticles; Nasal delivery; Vaccine.
Nanoparticles for nasal vaccination. Csaba N, Garcia-Fuentes M, Alonso MJ.Csaba N, et al.Adv Drug Deliv Rev. 2009 Feb 27;61(2):140-57. doi: 10.1016/j.addr.2008.09.005. Epub 2008 Dec 13.Adv Drug Deliv Rev. 2009.PMID: 19121350 Review.
Nanoparticulate systems for nasal delivery of drugs: a real improvement over simple systems? Illum L.Illum L.J Pharm Sci. 2007 Mar;96(3):473-83. doi: 10.1002/jps.20718.J Pharm Sci. 2007.PMID: 17117404 Review.
Pharmaceutical aspects of intranasal delivery of vaccines using particulate systems. Sharma S, Mukkur TK, Benson HA, Chen Y.Sharma S, et al.J Pharm Sci. 2009 Mar;98(3):812-43. doi: 10.1002/jps.21493.J Pharm Sci. 2009.PMID: 18661544 Review.
Nanoemulsion-based intranasal drug delivery system of saquinavir mesylate for brain targeting. Mahajan HS, Mahajan MS, Nerkar PP, Agrawal A.Mahajan HS, et al.Drug Deliv. 2014 Mar;21(2):148-54. doi: 10.3109/10717544.2013.838014. Epub 2013 Oct 16.Drug Deliv. 2014.PMID: 24128122
The application of mucoadhesive polymers in nasal drug delivery. Jiang L, Gao L, Wang X, Tang L, Ma J.Jiang L, et al.Drug Dev Ind Pharm. 2010 Mar;36(3):323-36. doi: 10.1080/03639040903170750.Drug Dev Ind Pharm. 2010.PMID: 19735210 Review.
Interleukin-4-loaded hydrogel scaffold regulates macrophages polarization to promote bone mesenchymal stem cells osteogenic differentiation via TGF-β1/Smad pathway for repair of bone defect. Zhang J, Shi H, Zhang N, Hu L, Jing W, Pan J.Zhang J, et al.Cell Prolif. 2020 Oct;53(10):e12907. doi: 10.1111/cpr.12907. Epub 2020 Sep 19.Cell Prolif. 2020.PMID: 32951298 Free PMC article.
Application of Nanopharmaceutics for Flibanserin Brain Delivery Augmentation Via the Nasal Route. Ahmed OAA, Fahmy UA, Badr-Eldin SM, Aldawsari HM, Awan ZA, Asfour HZ, Kammoun AK, Caruso G, Caraci F, Alfarsi A, Al-Ghamdi RA, Al-Ghamdi RA, Alhakamy NA.Ahmed OAA, et al.Nanomaterials (Basel). 2020 Jun 29;10(7):1270. doi: 10.3390/nano10071270.Nanomaterials (Basel). 2020.PMID: 32610539 Free PMC article.
Opioid antagonists as potential therapeutics for ischemic stroke. Peyravian N, Dikici E, Deo S, Toborek M, Daunert S.Peyravian N, et al.Prog Neurobiol. 2019 Nov;182:101679. doi: 10.1016/j.pneurobio.2019.101679. Epub 2019 Aug 6.Prog Neurobiol. 2019.PMID: 31398359 Free PMC article. Review.
Stimulus-responsive polymeric nanogels as smart drug delivery systems. Hajebi S, Rabiee N, Bagherzadeh M, Ahmadi S, Rabiee M, Roghani-Mamaqani H, Tahriri M, Tayebi L, Hamblin MR.Hajebi S, et al.Acta Biomater. 2019 Jul 1;92:1-18. doi: 10.1016/j.actbio.2019.05.018. Epub 2019 May 13.Acta Biomater. 2019.PMID: 31096042 Free PMC article. Review.
Preparation and Property Evaluation of Conductive Hydrogel Using Poly (Vinyl Alcohol)/Polyethylene Glycol/Graphene Oxide for Human Electrocardiogram Acquisition. Xiao X, Wu G, Zhou H, Qian K, Hu J.Xiao X, et al.Polymers (Basel). 2017 Jun 30;9(7):259. doi: 10.3390/polym9070259.Polymers (Basel). 2017.PMID: 30970936 Free PMC article.