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Accredited Drug Testing provides a full suite of drug and alcohol testing services at our 5 testing locations in the Carrabassett Valley, Maine region. We offer both DOT and non-DOT urine tests, breath alcohol tests, EtG alcohol testing, as well as hair drug tests for personal, business, and legal purposes. Rapid results and SAMSA certified lab analysis are both accessible in Carrabassett Valley, ME. Same-day services are available, with most testing centers just minutes away from your home or workplace. Additional offerings include Occupational Health Testing, Clinical Testing, and Background Checks.
Call (800) 221-4291 or register online. Choose your desired test and location conveniently for personal use, your staff, or others. Organizing a test is quick and simple; contact our scheduling team or arrange online at any hour. Our efficient and user-friendly process makes it easy to set up drug testing near Carrabassett Valley without any hassle.
* 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 Carrabassett Valley 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.
Carrabassett Valley, located in Franklin County, has seen a rise in opioid overdoses over the past few years.
A 2021 report indicated that Franklin County had an estimated 15% increase in drug-related ER visits.
Local law enforcement in Carrabassett Valley reported a 20% increase in drug-related arrests from 2019 to 2022.
In 2022, Franklin County had one of the higher rates of opioid prescriptions per capita in Maine.
Carrabassett Valley schools noted an uptick in juvenile drug-related incidents by approximately 10% from the previous year.
Franklin County's support centers saw a 25% rise in people seeking help for substance abuse in 2022.
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 Carrabassett Valley, ME, are increasingly adopting drug testing policies to maintain a safe workplace, consistent with state regulations ([Maine Department of Labor](https://www.maine.gov/labor/) - target='_blank'). Drug testing policies may include pre-employment screens and random testing for current employees.
These policies underscore a commitment to safety and highlight the potential risks of drug abuse affecting workplace productivity and employee health. Employers are encouraged to provide support and resources for employees struggling with addiction through employee assistance programs (EAPs) and partnerships with local support services.
The government of Carrabassett Valley, supported by Franklin County, has implemented several initiatives to combat drug abuse. Collaboration with state-level initiatives, such as the Maine Office of Substance Abuse and Mental Health Services (link), ensures a coordinated approach to tackling this issue.
Ongoing public awareness campaigns aim to prevent substance abuse and promote the services available to those in need in Carrabassett Valley. Additionally, funding has been increased for local law enforcement to improve drug-related crime responses and preventive education in schools.
Recent drug-related events in Carrabassett Valley have included several significant drug busts, emphasizing the ongoing battle against drug trafficking in the area. In one notable incident, Franklin County law enforcement conducted a coordinated raid resulting in multiple arrests and the seizure of substantial quantities of illicit substances.
These events underscore the effectiveness of increased law enforcement activities and community vigilance in reporting suspicious activities. They also serve as reminders of the pressing need for ongoing community efforts to prevent drug abuse and support recovery initiatives.
Accredited Drug Testing offers fast, reliable employment screening services in Carrabassett Valley, ME. Trusted by employers nationwide for accurate results and exceptional service.
Maine Office of Substance Abuse and Mental Health Services
211 Maine
Portland Recovery Community Center
Maine Alliance for Addiction Recovery
Maine Drug Data Hub
Maine Drug Services
Northern Light Acadia Hospital
MaineHealth Substance Use Treatment
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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