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Accredited Drug Testing delivers extensive drug and alcohol testing solutions at our 2 testing sites located in the Portage Creek, Alaska region. We conduct DOT and non-DOT urine drug screenings, breath alcohol exams, EtG alcohol tests, and hair analysis for personal, corporate, and legal requirements. In Portage Creek, AK, we provide rapid test results and utilize SAMSA-accredited lab services, with same-day appointments available. Most testing centers in Portage Creek are conveniently close to your home or workplace. More offerings include Occupational Health Testing, Clinical Exams, and Employment Background Checks.
Dial (800) 221-4291 or register via our website. Pick your preferred test and select a nearby facility—appointments are open for personal, employee, or third-party testing. Scheduling is swift and hassle-free; contact our scheduling team or make your appointment online 24/7. Our efficient, straightforward process ensures easy drug test arrangement near Portage Creek.
* You must register by phone or online to receive your donor pass/registration prior to proceeding to the testing center. You must bring a valid government issued ID along with the registration/barcode number which was sent to you by email.
When you're searching for drug testing near me or drug testing locations, we provide a simple and convenient process to find a drug and alcohol testing location near you that is certified to provide all of your drug and alcohol testing needs.
At our Portage Creek drug testing collection sites, Accredited Drug Testing provides one of the widest selections of drug and alcohol testing services available. Whether you're an employer, attorney, court, or private individual, we offer both DOT and non-DOT testing options—ranging from rapid tests to comprehensive lab-based screenings—capable of detecting nearly any substance.
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If you're an employer needing to test 25 or more employees and looking to save time and money, we offer mobile on-site drug testing where we come to you. Call us today for more information.
Drug elimination is the sum of the processes of removing an administered drug from the body. In the pharmacokinetic ADME scheme (absorption, distribution, metabolism, and excretion), it is frequently considered to encompass both metabolism and excretion. Hydrophobic drugs, to be excreted, must undergo metabolic modification making them more polar. Hydrophilic drugs, on the other hand, can undergo excretion directly, without the need for metabolic changes to their molecular structures.
Although many sites of metabolism and excretion exist, the chief organ of metabolism is the liver, while the organ primarily tasked with excretion is the kidney. Any significant dysfunction in either organ can result in the accumulation of the drug or its metabolites in toxic concentrations.
A variety of other factors impact elimination — intrinsic drug properties, such as polarity, size, or pKa. Also other factors include genetic variation among individuals, disease states affecting other organs, and pathways involved in the way the drug distributes through the body, such as first-pass metabolism.
Drug elimination is the removal of an administered drug from the body. It is accomplished in two ways, either by excretion of an unmetabolized drug in its intact form or by metabolic biotransformation followed by excretion. While excretion is primarily carried out by the kidneys, other organ systems are involved as well. Similarly, the liver is the primary site of biotransformation, yet extrahepatic metabolism takes place in a variety of organ systems affecting multiple drugs.
Given the multiple organ systems and the variety of metabolic transformations present, drug elimination can entail a significant degree of complexity. Hydrophilic drugs are typically directly excreted by the kidneys, while hydrophobic drugs undergo biotransformation before excretion. The purpose here is twofold – biotransformation serves both detoxify the exogenous substances as well as to increase their hydrophilicity, ensuring their elimination via the kidneys.
Two broad metabolic pathways of hepatic drug transformation exist. Phase I is the direct modification of the target molecule, whereas phase II entails conjugation of the target to a polar molecule of low molecular weight. Phase I prepare the drug to enter phase II, but single-phase metabolism also exists.
Phase I involves oxidation, reduction, and hydrolysis of the exogenous molecule. These reactions are accomplished by hepatic microsomal enzymes, which reside in the smooth endoplasmic reticulum of the hepatocytes. Best known among them is the cytochrome P450 system, whose enzymes are predominantly involved in oxidative metabolism. Within the cytochrome P450 family (CYP), the enzyme responsible for the metabolism of more than 50% of existing drugs is the CYP3A4. Its activity encompasses various classes of medications, including opioids, immunosuppressants, antihistamines, and benzodiazepines. The enzymes can also be induced or inhibited by a variety of substances they interact with, including pharmaceuticals. The increase in metabolic activity with CYP induction results in a diminished activity of drugs targeted by that particular isoform. Conversely, CYP inhibition will result in increased drug plasma concentration, potentially leading toxicity. The CYP3A4 is induced by phenytoin, phenobarbital, and St. John's wort, while diltiazem, erythromycin, and grapefruit inhibit it. Caution is, therefore, necessary when administering CYP3A4-metabolized drugs in the presence of any of the inhibitors or inducers.
Phase II consists of covalent bonding of polar groups to nonpolar molecules to render them water-soluble and allow renal or biliary excretion. Target molecules enter phase II directly or via initial processing through phase I. A variety of polar adjuncts is transferred, including amino acids, glucuronic acid, glutathione, acetate, and sulfate. Glucuronidation is one of the major pathways of phase II biotransformation. The UDP-glucuronosyltransferase (UGT) enzyme family performs this activity. Typically, glucuronide derivatives possess less or no activity of the original drug, but in some cases, pharmacologically active compounds result. Morphine-6-glucuronide is a phase II metabolite of morphine with significant analgesic activity. As with the CYP enzymes, inducers, and inhibitors of phase II, enzymes exist and may influence the efficacy of drugs that rely on conjugation before excretion.
The first-pass effect is a feature of hepatic metabolism that also plays a role in the elimination of multiple drugs. Here, the enteric consumed drugs are exposed directly to the liver via the portal vein, where they undergo biotransformation before entering the systemic circulation. This activity reduces the bioavailability and needs to be factored into the dose administered to the patient. Intravenously administered drugs are not subject to the first-pass effect.
Extrahepatic drug metabolism takes place in the GI tract, kidneys, lungs, plasma, and skin.
Renal excretion completes the process of elimination that begins in the liver. Polar drugs or their metabolites get filtered in the kidneys and typically do not undergo reabsorption. They subsequently get excreted in the urine. Urinary pH has a significant impact on excretion, as drug ionization changes depending on the alkaline or acidic environment. Increased excretion occurs with weakly acidic drugs in basic urine and weakly basic drugs in acidic urine.
Excretion in the bile is another significant form of drug elimination. The liver can actively secrete ionized drugs with a molecular weight greater than 300 g/mol into bile, from where they reach the digestive tract and are either eliminated in feces or reabsorbed as part of the enterohepatic cycle.
Other pathways of excretion include the lungs, breast milk, sweat, saliva, and tears
Employers in Portage Creek, AK, like many across the state, adhere to strict drug testing policies to ensure a safe and productive work environment. These policies often include pre-employment screenings, random tests, and post-accident assessments. Such measures align with state standards to minimize workplace risks and liability. For more details, visit the Alaska Department of Labor and Workforce Development.
The implementation of drug testing policies in Portage Creek is supported by federal regulations that allow industries to maintain workplace safety. Employers may follow guidelines set forth by agencies to prevent substance abuse-related incidents. These protocols emphasize creating a healthy work atmosphere, promoting efficiency while reducing potential hazards. Learn more about these federal guidelines by visiting the Substance Abuse and Mental Health Services Administration.
Adherence to drug testing policies is not just about compliance for Portage Creek employers but also about fostering a culture of trust. Employers are obliged to notify employees of these policies clearly and conduct tests fairly, respecting individual rights. This commitment to transparency helps in maintaining morale while ensuring regulatory adherence. For further understanding of state workplace laws and rights, check out the State of Alaska's official website.
In recent years, the government has intensified its efforts to combat drug issues in Portage Creek, AK. Local law enforcement, in collaboration with federal bodies like the Drug Enforcement Administration, has launched initiatives focused on curbing drug supply and distribution. These efforts are complemented by educational programs aimed at raising awareness about the dangers of drug misuse.
Additionally, partnerships with state-led organizations such as the Alaska Department of Health have been established to provide support and rehabilitation services for affected residents. By working closely with community leaders and public health officials, the government aims to reduce the impact of drug addiction and facilitate long-term recovery for individuals in Portage Creek.
Recently, law enforcement agencies in Portage Creek, AK, have intensified their efforts to crack down on the drug trade in the area. Through coordinated operations, they've successfully dismantled several local networks suspected of distributing illegal substances. These operations have not only disrupted the supply chains but have also led to the arrest of multiple individuals, highlighting the community's commitment to maintaining a safe and drug-free environment.
In a collaborative effort, Portage Creek's police department teamed up with state and federal agencies to address the growing concern of opioid misuse. Over a six-month period, this task force focused on identifying and shutting down distribution centers across the region. Their persistent endeavors have resulted in significant confiscations of both narcotics and related paraphernalia, showcasing the pressing need for continued vigilance and community support.
The local community in Portage Creek is beginning to see the positive impact of recent drug busts, which have been integral in promoting awareness and prevention measures. Public forums and educational workshops are being hosted to inform residents about the dangers of substance abuse. These initiatives serve to empower citizens with the knowledge needed to thwart potential drug-related issues before they escalate further.
Despite the recent successes in combating drug trafficking, officials in Portage Creek recognize the importance of ongoing preventive strategies. Efforts are being ramped up in schools to educate young people about the risks associated with drug use. By fostering open communication between students, parents, and educators, the community aims to build a solid foundation for a healthier future, free from the scourge of narcotics.
The ripple effect of the recent drug-related arrests in Portage Creek has extended to surrounding regions, inspiring similar crackdowns on illicit activities. By sharing intelligence with neighboring communities, law enforcement agencies are working to curb regional drug trafficking. This cooperative approach not only strengthens inter-community ties but also fortifies collective resolve against the pervasive influence of drugs.
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Time was running out before my Cdl got downgraded because of a violation I had on clearinghouse. I couldn't find an employer to send me for my return to duty test, but these guys had my test scheduled and done in the same day! They saved my cdl. Thank you again!
Michael Williams - 12/2/2024
I always have a good experience setting up company driver drug screens through ADT. I'm really happy I found them while searching online, they have made my job much easier.
Exodus Heath - 2/13/2025
I use their service for new hire and DOT employee's. Spoke with Taisha Walker this morning, and she was very helpful. She made the process smooth and seamless.
Christina Galdos - 3/9/2025