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At our 33 Sebago, Maine locations, Accredited Drug Testing provides a variety of drug and alcohol testing services. We conduct DOT and non-DOT urine screenings, breath alcohol examinations, as well as EtG and hair analysis for personal, corporate, and legal purposes. Rapid results and SAMSA certified lab analysis are offered with same day service, ensuring most Sebago sites are close to your home or work. Additional services encompass Occupational Health Checks, Clinical Testing, and Background Verification.
Dial (800) 221-4291 or sign up via our online portal. Opt for your test and pick a convenient center—whether it's for you, a staff member, or someone else, testing is accessible. With our straightforward procedure, arranging a drug test near Sebago is seamless. Scheduling is quick and simple; contact our team or book your test online anytime, any day.
* 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 Sebago 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.
DOT Drug Testing and Requirements
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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.
Sebago, located in Cumberland County, has seen a 15% increase in opioid overdoses from 2019 to 2021.
In 2020, Cumberland County reported 65 drug-related deaths, with Sebago contributing to 5% of this number.
A recent study in Sebago, Cumberland County, estimated that 8% of the population has engaged in non-prescribed opioid use.
Police records in Sebago, Cumberland County, show a 30% increase in drug-related arrests in 2021 compared to 2019.
Cumberland County has implemented several drug diversion programs, with notable participation from Sebago residents.
In Sebago, Cumberland County, Narcan kits distributed by local health agencies increased by 40% from 2020 to 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
In Sebago, ME, employers are increasingly implementing strict drug testing policies to ensure workplace safety and productivity. Many local businesses require pre-employment testing and routine checks in compliance with state laws. The Maine Department of Labor provides guidelines for these policies.
These drug testing initiatives are part of a broader strategy to deter substance abuse among employees. Employers partner with external agencies for testing services and support to maintain a drug-free environment. Such measures aim to reduce the negative impact of drug abuse on workforce efficiency and health.
The government of Sebago, ME, in conjunction with Cumberland County, has implemented several initiatives to combat drug abuse. These include increased funding for treatment programs and educational campaigns aimed at prevention. The Maine Department of Health and Human Services plays a vital role in these efforts.
Further programs initiated by the local government focus on collaboration with law enforcement and community organizations to address the root causes of addiction. Additionally, the Maine Center for Disease Control and Prevention works closely with Sebago officials to provide resources and educational materials.
Local law enforcement in Sebago, ME, regularly conducts operations to curb drug trafficking and abuse. In early 2023, a significant drug bust in Sebago led to multiple arrests and the seizure of large quantities of opioids. These efforts align with Cumberland County's broader initiatives against drug-related crime.
Community events are also organized to raise awareness about the dangers of drug abuse and promote rehabilitation. These events often involve collaborative efforts by local health agencies, law enforcement, and community groups, contributing to a more informed and resilient community.
Accredited Drug Testing offers fast, reliable employment screening services in Sebago, ME. Trusted by employers nationwide for accurate results and exceptional service.
Maine DHHS Substance Abuse and Mental Health Services
Amistad Peer Support and Recovery
Portland Recovery Community Center
Maine DHHS Mental Health Services
Northern Maine Recovery Collaborative
Maine's Crisis Support and Suicide Prevention
Bath-Brunswick BAOC
Kennebec Behavioral Health
Maine AllCare
Recovery Connections of Maine
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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